Canonical Allele Identifier: CA624662804

Gene: AIPL1

Linked Data

• dbSNP Id: rs1420425668
• gnomAD v2: 17-6328591-A-G
• gnomAD v4: 17-6425271-A-G
• MyVariant Identifiers: chr17:g.6328591A>G (hg19) ; chr17:g.6425271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425271A>G , CM000679.2:g.6425271A>G	GRCh38
NC_000017.10:g.6328591A>G , CM000679.1:g.6328591A>G	GRCh37
NC_000017.9:g.6269315A>G	NCBI36
NG_008474.1:g.14929T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.*189T>C MANE Select	ENSP00000370521.3:n.*189T>C
ENST00000250087.9:c.*189T>C	ENSP00000250087.5:n.*189T>C
ENST00000381128.2:c.*1216T>C	ENSP00000370520.2:n.*1216T>C
ENST00000381129.7:c.*189T>C	ENSP00000370521.3:n.*189T>C
ENST00000570584.5:c.251+8648T>C
ENST00000574506.5:c.*189T>C	ENSP00000458456.1:n.*189T>C
NM_001033054.2:c.*189T>C	NP_001028226.1:n.*189T>C
NM_001033055.2:c.*189T>C	NP_001028227.1:n.*189T>C
NM_001285399.2:c.*189T>C	NP_001272328.1:n.*189T>C
NM_001285400.2:c.*189T>C	NP_001272329.1:n.*189T>C
NM_001285401.2:c.*189T>C	NP_001272330.1:n.*189T>C
NM_001285402.1:c.*189T>C	NP_001272331.1:n.*189T>C
NM_014336.4:c.*189T>C	NP_055151.3:n.*189T>C
NM_001033054.3:c.*189T>C	NP_001028226.1:n.*189T>C
NM_001033055.3:c.*189T>C	NP_001028227.1:n.*189T>C
NM_001285399.3:c.*189T>C	NP_001272328.1:n.*189T>C
NM_001285400.3:c.*189T>C	NP_001272329.1:n.*189T>C
NM_001285401.3:c.*189T>C	NP_001272330.1:n.*189T>C
NM_001285402.2:c.*189T>C	NP_001272331.1:n.*189T>C
NM_014336.5:c.*189T>C MANE Select	NP_055151.3:n.*189T>C
NM_001285403.4:c.*1315T>C	NP_001272332.1:n.*1315T>C