Canonical Allele Identifier: CA452341378

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611570A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290432A>C , CM000668.2:g.135290432A>C	GRCh38
NC_000006.11:g.135611570A>C , CM000668.1:g.135611570A>C	GRCh37
NC_000006.10:g.135653263A>C	NCBI36
NG_008643.1:g.212334T>G
NG_008643.2:g.212334T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3579T>G MANE Select	ENSP00000265602.6:p.Thr1193=
ENST00000498558.6:n.620T>G
ENST00000527681.2:c.1248T>G
ENST00000679434.1:c.5195T>G	ENSP00000505592.1:n.5195T>G
ENST00000679450.1:c.3318T>G	ENSP00000506494.1:p.Thr1106=
ENST00000679490.1:n.2954T>G
ENST00000679502.1:n.2361-4785T>G
ENST00000679589.1:c.*3607T>G	ENSP00000506644.1:n.*3607T>G
ENST00000679668.1:c.5111T>G	ENSP00000505364.1:n.5111T>G
ENST00000679672.1:c.*1554T>G	ENSP00000505697.1:n.*1554T>G
ENST00000679711.1:c.1873T>G
ENST00000679742.1:c.4896-4785T>G	ENSP00000504890.1:n.4896-4785T>G
ENST00000679890.1:n.2070T>G
ENST00000679925.1:c.3486-4785T>G	ENSP00000505502.1:n.3486-4785T>G
ENST00000679943.1:c.3640T>G	ENSP00000505663.1:n.3640T>G
ENST00000680071.1:n.4352T>G
ENST00000680119.1:c.3804T>G	ENSP00000506403.1:n.3804T>G
ENST00000680328.1:n.688T>G
ENST00000680337.1:c.944-4785T>G
ENST00000680561.1:n.6229-4785T>G
ENST00000680826.1:c.3764T>G	ENSP00000505224.1:n.3764T>G
ENST00000680840.1:c.3807T>G	ENSP00000505809.1:n.3807T>G
ENST00000680965.1:c.*1033T>G	ENSP00000505398.1:n.*1033T>G
ENST00000681022.1:c.3579T>G	ENSP00000505121.1:p.Thr1193=
ENST00000681057.1:n.2744-4785T>G
ENST00000681196.1:n.4259-4785T>G
ENST00000681301.1:c.3426T>G	ENSP00000505093.1:p.Thr1142=
ENST00000681331.1:n.1308T>G
ENST00000681332.1:n.4096T>G
ENST00000681340.1:c.3579T>G	ENSP00000505666.1:p.Thr1193=
ENST00000681365.1:c.3579T>G	ENSP00000506604.1:p.Thr1193=
ENST00000681488.1:c.3448T>G	ENSP00000505884.1:n.3448T>G
ENST00000681522.1:c.3579T>G	ENSP00000506005.1:p.Thr1193=
ENST00000681556.1:n.3713T>G
ENST00000681718.1:c.*2066T>G	ENSP00000505266.1:n.*2066T>G
ENST00000681754.1:n.4267T>G
ENST00000681828.1:c.5135T>G	ENSP00000505608.1:n.5135T>G
ENST00000681841.1:c.3579T>G	ENSP00000504965.1:p.Thr1193=
ENST00000681860.1:c.3395T>G	ENSP00000506250.1:n.3395T>G
ENST00000265602.10:c.3579T>G	ENSP00000265602.6:p.Thr1193=
ENST00000367799.6:c.1985-4785T>G
ENST00000367800.8:c.3579T>G	ENSP00000356774.4:p.Thr1193=
ENST00000457866.6:c.3579T>G	ENSP00000388650.2:p.Thr1193=
ENST00000475846.6:c.2009T>G
ENST00000487135.1:n.155-4785T>G
ENST00000498558.5:n.428T>G
ENST00000527681.1:c.188T>G
NM_001134830.1:c.3579T>G	NP_001128302.1:p.Thr1193=
NM_001134831.1:c.3579T>G	NP_001128303.1:p.Thr1193=
NM_017651.4:c.3579T>G	NP_060121.3:p.Thr1193=
XM_011535910.1:c.3579T>G	XP_011534212.1:p.Thr1193=
XM_011535911.1:c.3579T>G	XP_011534213.1:p.Thr1193=
XM_011535915.1:c.3486-4785T>G	XP_011534217.1:n.3486-4785T>G
XR_942488.1:n.5421T>G
XR_942490.1:n.5328-4785T>G
XR_942493.1:n.5282T>G
XR_942494.1:n.5119T>G
NM_001350503.1:c.3579T>G	NP_001337432.1:p.Thr1193=
NM_001350504.1:c.3486-4785T>G	NP_001337433.1:n.3486-4785T>G
XM_011535910.3:c.3579T>G	XP_011534212.1:p.Thr1193=
XM_011535911.3:c.3579T>G	XP_011534213.1:p.Thr1193=
XM_017010980.2:c.*100T>G	XP_016866469.1:n.*100T>G
XM_017010981.2:c.3525T>G	XP_016866470.1:p.Thr1175=
XM_024446479.1:c.3525T>G	XP_024302247.1:p.Thr1175=
XR_001743479.2:n.5518T>G
XR_001743480.2:n.4346T>G
XR_001743481.2:n.4311T>G
XR_001743482.2:n.4214T>G
XR_001743483.2:n.5425-4785T>G
XR_001743484.2:n.5379T>G
XR_001743485.2:n.4075T>G
XR_001743486.2:n.5286-4785T>G
XR_001743487.2:n.5501T>G
XR_001743488.1:n.5743T>G
XR_001743489.2:n.5216T>G
XR_001743490.2:n.4197T>G
XR_002956286.1:n.3850T>G
XR_002956287.1:n.3757-4785T>G
NM_001134831.2:c.3579T>G MANE Select	NP_001128303.1:p.Thr1193=
NM_001134830.2:c.3579T>G	NP_001128302.1:p.Thr1193=
NM_001350503.2:c.3579T>G	NP_001337432.1:p.Thr1193=
NM_001350504.2:c.3486-4785T>G	NP_001337433.1:n.3486-4785T>G
NM_017651.5:c.3579T>G	NP_060121.3:p.Thr1193=