Canonical Allele Identifier: CA397394175

Gene: AIPL1

Linked Data

• ClinVar Variation Id: 1939858
• ClinVar RCV Id: RCV002650220
• gnomAD v4: 17-6425468-G-A
• MyVariant Identifiers: chr17:g.6328788G>A (hg19) ; chr17:g.6425468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425468G>A , CM000679.2:g.6425468G>A	GRCh38
NC_000017.10:g.6328788G>A , CM000679.1:g.6328788G>A	GRCh37
NC_000017.9:g.6269512G>A	NCBI36
NG_008474.1:g.14732C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1147C>T MANE Select	ENSP00000370521.3:p.Gln383Ter
ENST00000250087.9:c.958C>T	ENSP00000250087.5:p.Gln320Ter
ENST00000381128.2:c.*1019C>T	ENSP00000370520.2:n.*1019C>T
ENST00000381129.7:c.1147C>T	ENSP00000370521.3:p.Gln383Ter
ENST00000570466.5:c.1081C>T	ENSP00000461287.1:p.Gln361Ter
ENST00000570584.5:c.251+8451C>T
ENST00000574506.5:c.1111C>T	ENSP00000458456.1:p.Gln371Ter
ENST00000575265.5:c.*1118C>T	ENSP00000459673.1:n.*1118C>T
ENST00000576307.5:c.967C>T	ENSP00000459522.1:p.Gln323Ter
ENST00000576776.5:c.1075C>T	ENSP00000460827.1:p.Gln359Ter
ENST00000621374.4:c.*165C>T	ENSP00000481337.1:n.*165C>T
NM_001033054.2:c.958C>T	NP_001028226.1:p.Gln320Ter
NM_001033055.2:c.967C>T	NP_001028227.1:p.Gln323Ter
NM_001285399.2:c.1111C>T	NP_001272328.1:p.Gln371Ter
NM_001285400.2:c.1081C>T	NP_001272329.1:p.Gln361Ter
NM_001285401.2:c.1075C>T	NP_001272330.1:p.Gln359Ter
NM_001285402.1:c.1030C>T	NP_001272331.1:p.Gln344Ter
NM_014336.4:c.1147C>T	NP_055151.3:p.Gln383Ter
NM_001033054.3:c.958C>T	NP_001028226.1:p.Gln320Ter
NM_001033055.3:c.967C>T	NP_001028227.1:p.Gln323Ter
NM_001285399.3:c.1111C>T	NP_001272328.1:p.Gln371Ter
NM_001285400.3:c.1081C>T	NP_001272329.1:p.Gln361Ter
NM_001285401.3:c.1075C>T	NP_001272330.1:p.Gln359Ter
NM_001285402.2:c.1030C>T	NP_001272331.1:p.Gln344Ter
NM_001285403.3:c.*1118C>T	NP_001272332.1:n.*1118C>T
NM_014336.5:c.1147C>T MANE Select	NP_055151.3:p.Gln383Ter
NM_001285403.4:c.*1118C>T	NP_001272332.1:n.*1118C>T