Canonical Allele Identifier: CA452341402

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611609T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290471T>G , CM000668.2:g.135290471T>G	GRCh38
NC_000006.11:g.135611609T>G , CM000668.1:g.135611609T>G	GRCh37
NC_000006.10:g.135653302T>G	NCBI36
NG_008643.1:g.212295A>C
NG_008643.2:g.212295A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265602.11:c.3540A>C MANE Select	ENSP00000265602.6:p.Thr1180=
ENST00000498558.6:n.581A>C
ENST00000527681.2:c.1209A>C
ENST00000679434.1:c.5156A>C	ENSP00000505592.1:n.5156A>C
ENST00000679450.1:c.3279A>C	ENSP00000506494.1:p.Thr1093=
ENST00000679490.1:n.2915A>C
ENST00000679502.1:n.2361-4824A>C
ENST00000679589.1:c.*3568A>C	ENSP00000506644.1:n.*3568A>C
ENST00000679668.1:c.5072A>C	ENSP00000505364.1:n.5072A>C
ENST00000679672.1:c.*1515A>C	ENSP00000505697.1:n.*1515A>C
ENST00000679711.1:c.1834A>C
ENST00000679742.1:c.4896-4824A>C	ENSP00000504890.1:n.4896-4824A>C
ENST00000679890.1:n.2031A>C
ENST00000679925.1:c.3486-4824A>C	ENSP00000505502.1:n.3486-4824A>C
ENST00000679943.1:c.3601A>C	ENSP00000505663.1:n.3601A>C
ENST00000680071.1:n.4313A>C
ENST00000680119.1:c.3765A>C	ENSP00000506403.1:n.3765A>C
ENST00000680328.1:n.649A>C
ENST00000680337.1:c.944-4824A>C
ENST00000680561.1:n.6229-4824A>C
ENST00000680826.1:c.3725A>C	ENSP00000505224.1:n.3725A>C
ENST00000680840.1:c.3768A>C	ENSP00000505809.1:n.3768A>C
ENST00000680965.1:c.*994A>C	ENSP00000505398.1:n.*994A>C
ENST00000681022.1:c.3540A>C	ENSP00000505121.1:p.Thr1180=
ENST00000681057.1:n.2744-4824A>C
ENST00000681196.1:n.4259-4824A>C
ENST00000681301.1:c.3387A>C	ENSP00000505093.1:p.Thr1129=
ENST00000681331.1:n.1269A>C
ENST00000681332.1:n.4057A>C
ENST00000681340.1:c.3540A>C	ENSP00000505666.1:p.Thr1180=
ENST00000681365.1:c.3540A>C	ENSP00000506604.1:p.Thr1180=
ENST00000681488.1:c.3409A>C	ENSP00000505884.1:n.3409A>C
ENST00000681522.1:c.3540A>C	ENSP00000506005.1:p.Thr1180=
ENST00000681556.1:n.3674A>C
ENST00000681718.1:c.*2027A>C	ENSP00000505266.1:n.*2027A>C
ENST00000681754.1:n.4228A>C
ENST00000681828.1:c.5096A>C	ENSP00000505608.1:n.5096A>C
ENST00000681841.1:c.3540A>C	ENSP00000504965.1:p.Thr1180=
ENST00000681860.1:c.3356A>C	ENSP00000506250.1:n.3356A>C
ENST00000265602.10:c.3540A>C	ENSP00000265602.6:p.Thr1180=
ENST00000367799.6:c.1985-4824A>C
ENST00000367800.8:c.3540A>C	ENSP00000356774.4:p.Thr1180=
ENST00000457866.6:c.3540A>C	ENSP00000388650.2:p.Thr1180=
ENST00000475846.6:c.1970A>C
ENST00000487135.1:n.155-4824A>C
ENST00000498558.5:n.389A>C
ENST00000527681.1:c.149A>C
NM_001134830.1:c.3540A>C	NP_001128302.1:p.Thr1180=
NM_001134831.1:c.3540A>C	NP_001128303.1:p.Thr1180=
NM_017651.4:c.3540A>C	NP_060121.3:p.Thr1180=
XM_011535910.1:c.3540A>C	XP_011534212.1:p.Thr1180=
XM_011535911.1:c.3540A>C	XP_011534213.1:p.Thr1180=
XM_011535914.1:c.*61A>C	XP_011534216.1:n.*61A>C
XM_011535915.1:c.3486-4824A>C	XP_011534217.1:n.3486-4824A>C
XR_942488.1:n.5382A>C
XR_942490.1:n.5328-4824A>C
XR_942493.1:n.5243A>C
XR_942494.1:n.5080A>C
NM_001350503.1:c.3540A>C	NP_001337432.1:p.Thr1180=
NM_001350504.1:c.3486-4824A>C	NP_001337433.1:n.3486-4824A>C
XM_011535910.3:c.3540A>C	XP_011534212.1:p.Thr1180=
XM_011535911.3:c.3540A>C	XP_011534213.1:p.Thr1180=
XM_017010980.2:c.*61A>C	XP_016866469.1:n.*61A>C
XM_017010981.2:c.3486A>C	XP_016866470.1:p.Thr1162=
XM_024446479.1:c.3486A>C	XP_024302247.1:p.Thr1162=
XR_001743479.2:n.5479A>C
XR_001743480.2:n.4307A>C
XR_001743481.2:n.4272A>C
XR_001743482.2:n.4175A>C
XR_001743483.2:n.5425-4824A>C
XR_001743484.2:n.5340A>C
XR_001743485.2:n.4036A>C
XR_001743486.2:n.5286-4824A>C
XR_001743487.2:n.5462A>C
XR_001743488.1:n.5704A>C
XR_001743489.2:n.5177A>C
XR_001743490.2:n.4158A>C
XR_002956286.1:n.3811A>C
XR_002956287.1:n.3757-4824A>C
NM_001134831.2:c.3540A>C MANE Select	NP_001128303.1:p.Thr1180=
NM_001134830.2:c.3540A>C	NP_001128302.1:p.Thr1180=
NM_001350503.2:c.3540A>C	NP_001337432.1:p.Thr1180=
NM_001350504.2:c.3486-4824A>C	NP_001337433.1:n.3486-4824A>C
NM_017651.5:c.3540A>C	NP_060121.3:p.Thr1180=