Canonical Allele Identifier: CA365840961

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611654C>G (hg19) ; chr6:g.135290516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290516C>G , CM000668.2:g.135290516C>G	GRCh38
NC_000006.11:g.135611654C>G , CM000668.1:g.135611654C>G	GRCh37
NC_000006.10:g.135653347C>G	NCBI36
NG_008643.1:g.212250G>C
NG_008643.2:g.212250G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3495G>C MANE Select	ENSP00000265602.6:p.Met1165Ile
ENST00000498558.6:n.536G>C
ENST00000527681.2:c.1164G>C
ENST00000679434.1:c.5111G>C	ENSP00000505592.1:n.5111G>C
ENST00000679450.1:c.3234G>C	ENSP00000506494.1:p.Met1078Ile
ENST00000679490.1:n.2870G>C
ENST00000679502.1:n.2361-4869G>C
ENST00000679589.1:c.*3523G>C	ENSP00000506644.1:n.*3523G>C
ENST00000679668.1:c.5027G>C	ENSP00000505364.1:n.5027G>C
ENST00000679672.1:c.*1470G>C	ENSP00000505697.1:n.*1470G>C
ENST00000679711.1:c.1789G>C
ENST00000679742.1:c.4896-4869G>C	ENSP00000504890.1:n.4896-4869G>C
ENST00000679890.1:n.1986G>C
ENST00000679925.1:c.3486-4869G>C	ENSP00000505502.1:n.3486-4869G>C
ENST00000679943.1:c.3556G>C	ENSP00000505663.1:n.3556G>C
ENST00000680071.1:n.4268G>C
ENST00000680119.1:c.3720G>C	ENSP00000506403.1:n.3720G>C
ENST00000680328.1:n.604G>C
ENST00000680337.1:c.944-4869G>C
ENST00000680561.1:n.6229-4869G>C
ENST00000680826.1:c.3680G>C	ENSP00000505224.1:n.3680G>C
ENST00000680840.1:c.3723G>C	ENSP00000505809.1:n.3723G>C
ENST00000680965.1:c.*949G>C	ENSP00000505398.1:n.*949G>C
ENST00000681022.1:c.3495G>C	ENSP00000505121.1:p.Met1165Ile
ENST00000681057.1:n.2744-4869G>C
ENST00000681196.1:n.4259-4869G>C
ENST00000681301.1:c.3342G>C	ENSP00000505093.1:p.Met1114Ile
ENST00000681331.1:n.1224G>C
ENST00000681332.1:n.4012G>C
ENST00000681340.1:c.3495G>C	ENSP00000505666.1:p.Met1165Ile
ENST00000681365.1:c.3495G>C	ENSP00000506604.1:p.Met1165Ile
ENST00000681488.1:c.3364G>C	ENSP00000505884.1:n.3364G>C
ENST00000681522.1:c.3495G>C	ENSP00000506005.1:p.Met1165Ile
ENST00000681556.1:n.3629G>C
ENST00000681718.1:c.*1982G>C	ENSP00000505266.1:n.*1982G>C
ENST00000681754.1:n.4183G>C
ENST00000681828.1:c.5051G>C	ENSP00000505608.1:n.5051G>C
ENST00000681841.1:c.3495G>C	ENSP00000504965.1:p.Met1165Ile
ENST00000681860.1:c.3311G>C	ENSP00000506250.1:n.3311G>C
ENST00000265602.10:c.3495G>C	ENSP00000265602.6:p.Met1165Ile
ENST00000367799.6:c.1985-4869G>C
ENST00000367800.8:c.3495G>C	ENSP00000356774.4:p.Met1165Ile
ENST00000457866.6:c.3495G>C	ENSP00000388650.2:p.Met1165Ile
ENST00000475846.6:c.1925G>C
ENST00000487135.1:n.155-4869G>C
ENST00000498558.5:n.344G>C
ENST00000527681.1:c.104G>C
NM_001134830.1:c.3495G>C	NP_001128302.1:p.Met1165Ile
NM_001134831.1:c.3495G>C	NP_001128303.1:p.Met1165Ile
NM_017651.4:c.3495G>C	NP_060121.3:p.Met1165Ile
XM_011535910.1:c.3495G>C	XP_011534212.1:p.Met1165Ile
XM_011535911.1:c.3495G>C	XP_011534213.1:p.Met1165Ile
XM_011535914.1:c.*16G>C	XP_011534216.1:n.*16G>C
XM_011535915.1:c.3486-4869G>C	XP_011534217.1:n.3486-4869G>C
XR_942488.1:n.5337G>C
XR_942490.1:n.5328-4869G>C
XR_942493.1:n.5198G>C
XR_942494.1:n.5035G>C
NM_001350503.1:c.3495G>C	NP_001337432.1:p.Met1165Ile
NM_001350504.1:c.3486-4869G>C	NP_001337433.1:n.3486-4869G>C
XM_011535910.3:c.3495G>C	XP_011534212.1:p.Met1165Ile
XM_011535911.3:c.3495G>C	XP_011534213.1:p.Met1165Ile
XM_017010980.2:c.*16G>C	XP_016866469.1:n.*16G>C
XM_017010981.2:c.3441G>C	XP_016866470.1:p.Met1147Ile
XM_024446479.1:c.3441G>C	XP_024302247.1:p.Met1147Ile
XR_001743479.2:n.5434G>C
XR_001743480.2:n.4262G>C
XR_001743481.2:n.4227G>C
XR_001743482.2:n.4130G>C
XR_001743483.2:n.5425-4869G>C
XR_001743484.2:n.5295G>C
XR_001743485.2:n.3991G>C
XR_001743486.2:n.5286-4869G>C
XR_001743487.2:n.5417G>C
XR_001743488.1:n.5659G>C
XR_001743489.2:n.5132G>C
XR_001743490.2:n.4113G>C
XR_002956286.1:n.3766G>C
XR_002956287.1:n.3757-4869G>C
NM_001134831.2:c.3495G>C MANE Select	NP_001128303.1:p.Met1165Ile
NM_001134830.2:c.3495G>C	NP_001128302.1:p.Met1165Ile
NM_001350503.2:c.3495G>C	NP_001337432.1:p.Met1165Ile
NM_001350504.2:c.3486-4869G>C	NP_001337433.1:n.3486-4869G>C
NM_017651.5:c.3495G>C	NP_060121.3:p.Met1165Ile