Canonical Allele Identifier: CA397394632

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6329006T>G (hg19) ; chr17:g.6425686T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425686T>G , CM000679.2:g.6425686T>G	GRCh38
NC_000017.10:g.6329006T>G , CM000679.1:g.6329006T>G	GRCh37
NC_000017.9:g.6269730T>G	NCBI36
NG_008474.1:g.14514A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.929A>C MANE Select	ENSP00000370521.3:p.Asn310Thr
ENST00000250087.9:c.740A>C	ENSP00000250087.5:p.Asn247Thr
ENST00000381128.2:c.*801A>C	ENSP00000370520.2:n.*801A>C
ENST00000381129.7:c.929A>C	ENSP00000370521.3:p.Asn310Thr
ENST00000570466.5:c.863A>C	ENSP00000461287.1:p.Asn288Thr
ENST00000570584.5:c.251+8233A>C
ENST00000574506.5:c.893A>C	ENSP00000458456.1:p.Asn298Thr
ENST00000575265.5:c.*900A>C	ENSP00000459673.1:n.*900A>C
ENST00000576307.5:c.749A>C	ENSP00000459522.1:p.Asn250Thr
ENST00000576776.5:c.857A>C	ENSP00000460827.1:p.Asn286Thr
ENST00000621374.4:c.929A>C	ENSP00000481337.1:p.Asn310Thr
NM_001033054.2:c.740A>C	NP_001028226.1:p.Asn247Thr
NM_001033055.2:c.749A>C	NP_001028227.1:p.Asn250Thr
NM_001285399.2:c.893A>C	NP_001272328.1:p.Asn298Thr
NM_001285400.2:c.863A>C	NP_001272329.1:p.Asn288Thr
NM_001285401.2:c.857A>C	NP_001272330.1:p.Asn286Thr
NM_001285402.1:c.812A>C	NP_001272331.1:p.Asn271Thr
NM_014336.4:c.929A>C	NP_055151.3:p.Asn310Thr
NM_001033054.3:c.740A>C	NP_001028226.1:p.Asn247Thr
NM_001033055.3:c.749A>C	NP_001028227.1:p.Asn250Thr
NM_001285399.3:c.893A>C	NP_001272328.1:p.Asn298Thr
NM_001285400.3:c.863A>C	NP_001272329.1:p.Asn288Thr
NM_001285401.3:c.857A>C	NP_001272330.1:p.Asn286Thr
NM_001285402.2:c.812A>C	NP_001272331.1:p.Asn271Thr
NM_001285403.3:c.*900A>C	NP_001272332.1:n.*900A>C
NM_014336.5:c.929A>C MANE Select	NP_055151.3:p.Asn310Thr
NM_001285403.4:c.*900A>C	NP_001272332.1:n.*900A>C