Canonical Allele Identifier: CA397394261

Gene: AIPL1

Linked Data

• dbSNP Id: rs746453263
• gnomAD v2: 17-6328833-C-A
• gnomAD v4: 17-6425513-C-A
• MyVariant Identifiers: chr17:g.6328833C>A (hg19) ; chr17:g.6425513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425513C>A , CM000679.2:g.6425513C>A	GRCh38
NC_000017.10:g.6328833C>A , CM000679.1:g.6328833C>A	GRCh37
NC_000017.9:g.6269557C>A	NCBI36
NG_008474.1:g.14687G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1102G>T MANE Select	ENSP00000370521.3:p.Ala368Ser
ENST00000250087.9:c.913G>T	ENSP00000250087.5:p.Ala305Ser
ENST00000381128.2:c.*974G>T	ENSP00000370520.2:n.*974G>T
ENST00000381129.7:c.1102G>T	ENSP00000370521.3:p.Ala368Ser
ENST00000570466.5:c.1036G>T	ENSP00000461287.1:p.Ala346Ser
ENST00000570584.5:c.251+8406G>T
ENST00000574506.5:c.1066G>T	ENSP00000458456.1:p.Ala356Ser
ENST00000575265.5:c.*1073G>T	ENSP00000459673.1:n.*1073G>T
ENST00000576307.5:c.922G>T	ENSP00000459522.1:p.Ala308Ser
ENST00000576776.5:c.1030G>T	ENSP00000460827.1:p.Ala344Ser
ENST00000621374.4:c.*120G>T	ENSP00000481337.1:n.*120G>T
NM_001033054.2:c.913G>T	NP_001028226.1:p.Ala305Ser
NM_001033055.2:c.922G>T	NP_001028227.1:p.Ala308Ser
NM_001285399.2:c.1066G>T	NP_001272328.1:p.Ala356Ser
NM_001285400.2:c.1036G>T	NP_001272329.1:p.Ala346Ser
NM_001285401.2:c.1030G>T	NP_001272330.1:p.Ala344Ser
NM_001285402.1:c.985G>T	NP_001272331.1:p.Ala329Ser
NM_014336.4:c.1102G>T	NP_055151.3:p.Ala368Ser
NM_001033054.3:c.913G>T	NP_001028226.1:p.Ala305Ser
NM_001033055.3:c.922G>T	NP_001028227.1:p.Ala308Ser
NM_001285399.3:c.1066G>T	NP_001272328.1:p.Ala356Ser
NM_001285400.3:c.1036G>T	NP_001272329.1:p.Ala346Ser
NM_001285401.3:c.1030G>T	NP_001272330.1:p.Ala344Ser
NM_001285402.2:c.985G>T	NP_001272331.1:p.Ala329Ser
NM_001285403.3:c.*1073G>T	NP_001272332.1:n.*1073G>T
NM_014336.5:c.1102G>T MANE Select	NP_055151.3:p.Ala368Ser
NM_001285403.4:c.*1073G>T	NP_001272332.1:n.*1073G>T