Canonical Allele Identifier: CA1665857942
Gene: AHI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.135321573G= , CM000668.2:g.135321573G= GRCh38
NC_000006.11:g.135642711G= , CM000668.1:g.135642711G= GRCh37
NC_000006.10:g.135684404G= NCBI36
NG_008643.1:g.181193C=
NG_008643.2:g.181193C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265602.11:c.3328+1589C= MANE Select ENSP00000265602.6:n.3328+1589C=
ENST00000367799.7:c.2380+1589C= ENSP00000356773.3:n.2380+1589C=
ENST00000527681.2:c.997+1589C=
ENST00000679434.1:c.3513+1589C= ENSP00000505592.1:n.3513+1589C=
ENST00000679450.1:c.3166-21015C= ENSP00000506494.1:n.3166-21015C=
ENST00000679476.1:c.1257+1589C=
ENST00000679589.1:c.*3356+1589C= ENSP00000506644.1:n.*3356+1589C=
ENST00000679622.1:c.*255+1589C= ENSP00000506261.1:n.*255+1589C=
ENST00000679668.1:c.3450+1589C= ENSP00000505364.1:n.3450+1589C=
ENST00000679672.1:c.3328+1589C= ENSP00000505697.1:n.3328+1589C=
ENST00000679711.1:c.1622+1589C=
ENST00000679742.1:c.3328+1589C= ENSP00000504890.1:n.3328+1589C=
ENST00000679890.1:n.1819+1589C=
ENST00000679925.1:c.3328+1589C= ENSP00000505502.1:n.3328+1589C=
ENST00000679943.1:c.3328+1589C= ENSP00000505663.1:n.3328+1589C=
ENST00000680071.1:n.1842+1589C=
ENST00000680119.1:c.3405+1589C= ENSP00000506403.1:n.3405+1589C=
ENST00000680157.1:n.1842+1589C=
ENST00000680184.1:c.*117+1589C= ENSP00000506009.1:n.*117+1589C=
ENST00000680278.1:c.3800+1589C= ENSP00000506153.1:n.3800+1589C=
ENST00000680337.1:c.787-2957C=
ENST00000680561.1:n.6071+1589C=
ENST00000680656.1:c.*405+1589C= ENSP00000505297.1:n.*405+1589C=
ENST00000680826.1:c.3513+1589C= ENSP00000505224.1:n.3513+1589C=
ENST00000680840.1:c.3450+1589C= ENSP00000505809.1:n.3450+1589C=
ENST00000680965.1:c.*782+1589C= ENSP00000505398.1:n.*782+1589C=
ENST00000681022.1:c.3328+1589C= ENSP00000505121.1:n.3328+1589C=
ENST00000681057.1:n.2744-35926C=
ENST00000681196.1:n.1842+1589C=
ENST00000681301.1:c.3175+1589C= ENSP00000505093.1:n.3175+1589C=
ENST00000681331.1:n.1057+1589C=
ENST00000681332.1:n.3845+1589C=
ENST00000681340.1:c.3328+1589C= ENSP00000505666.1:n.3328+1589C=
ENST00000681365.1:c.3328+1589C= ENSP00000506604.1:n.3328+1589C=
ENST00000681488.1:c.3197+1589C= ENSP00000505884.1:n.3197+1589C=
ENST00000681522.1:c.3328+1589C= ENSP00000506005.1:n.3328+1589C=
ENST00000681670.1:c.3328+1589C= ENSP00000504895.1:n.3328+1589C=
ENST00000681718.1:c.*405+1589C= ENSP00000505266.1:n.*405+1589C=
ENST00000681756.1:c.3328+1589C= ENSP00000506505.1:n.3328+1589C=
ENST00000681828.1:c.3450+1589C= ENSP00000505608.1:n.3450+1589C=
ENST00000681841.1:c.3328+1589C= ENSP00000504965.1:n.3328+1589C=
ENST00000681860.1:c.2941+1589C= ENSP00000506250.1:n.2941+1589C=
ENST00000265602.10:c.3328+1589C= ENSP00000265602.6:n.3328+1589C=
ENST00000367799.6:c.1827+1589C=
ENST00000367800.8:c.3328+1589C= ENSP00000356774.4:n.3328+1589C=
ENST00000457866.6:c.3328+1589C= ENSP00000388650.2:n.3328+1589C=
ENST00000475846.6:c.1520+1589C=
ENST00000531788.5:c.*1369-2957C= ENSP00000432167.1:n.*1369-2957C=
ENST00000533029.1:n.218+1589C=
NM_001134830.1:c.3328+1589C= NP_001128302.1:n.3328+1589C=
NM_001134831.1:c.3328+1589C= NP_001128303.1:n.3328+1589C=
NM_017651.4:c.3328+1589C= NP_060121.3:n.3328+1589C=
XM_011535910.1:c.3328+1589C= XP_011534212.1:n.3328+1589C=
XM_011535911.1:c.3328+1589C= XP_011534213.1:n.3328+1589C=
XM_011535912.1:c.3328+1589C= XP_011534214.1:n.3328+1589C=
XM_011535913.1:c.3328+1589C= XP_011534215.1:n.3328+1589C=
XM_011535914.1:c.3328+1589C= XP_011534216.1:n.3328+1589C=
XM_011535915.1:c.3328+1589C= XP_011534217.1:n.3328+1589C=
XM_011535916.1:c.3166-2957C= XP_011534218.1:n.3166-2957C=
XR_942488.1:n.3621+1589C=
XR_942489.1:n.3621+1589C=
XR_942490.1:n.3621+1589C=
XR_942491.1:n.3621+1589C=
XR_942493.1:n.3621+1589C=
XR_942494.1:n.3459-2957C=
NM_001350503.1:c.3328+1589C= NP_001337432.1:n.3328+1589C=
NM_001350504.1:c.3328+1589C= NP_001337433.1:n.3328+1589C=
XM_011535910.3:c.3328+1589C= XP_011534212.1:n.3328+1589C=
XM_011535911.3:c.3328+1589C= XP_011534213.1:n.3328+1589C=
XM_017010978.2:c.3328+1589C= XP_016866467.1:n.3328+1589C=
XM_017010979.2:c.3328+1589C= XP_016866468.1:n.3328+1589C=
XM_017010980.2:c.3328+1589C= XP_016866469.1:n.3328+1589C=
XM_017010981.2:c.3274+1589C= XP_016866470.1:n.3274+1589C=
XM_024446479.1:c.3274+1589C= XP_024302247.1:n.3274+1589C=
XM_024446480.1:c.3166-2957C= XP_024302248.1:n.3166-2957C=
XR_001743479.2:n.3718+1589C=
XR_001743480.2:n.3718+1589C=
XR_001743481.2:n.3718+1589C=
XR_001743482.2:n.3718+1589C=
XR_001743483.2:n.3718+1589C=
XR_001743484.2:n.3718+1589C=
XR_001743485.2:n.3718+1589C=
XR_001743486.2:n.3718+1589C=
XR_001743487.2:n.3840+1589C=
XR_001743488.1:n.4082+1589C=
XR_001743489.2:n.3556-2957C=
XR_001743490.2:n.3840+1589C=
XR_002956286.1:n.3599+1589C=
XR_002956287.1:n.3599+1589C=
NM_001134831.2:c.3328+1589C= MANE Select NP_001128303.1:n.3328+1589C=
NM_001134830.2:c.3328+1589C= NP_001128302.1:n.3328+1589C=
NM_001350503.2:c.3328+1589C= NP_001337432.1:n.3328+1589C=
NM_001350504.2:c.3328+1589C= NP_001337433.1:n.3328+1589C=
NM_017651.5:c.3328+1589C= NP_060121.3:n.3328+1589C=