Canonical Allele Identifier: CA397394394

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425582-G-C
• MyVariant Identifiers: chr17:g.6328902G>C (hg19) ; chr17:g.6425582G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425582G>C , CM000679.2:g.6425582G>C	GRCh38
NC_000017.10:g.6328902G>C , CM000679.1:g.6328902G>C	GRCh37
NC_000017.9:g.6269626G>C	NCBI36
NG_008474.1:g.14618C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1033C>G MANE Select	ENSP00000370521.3:p.Gln345Glu
ENST00000250087.9:c.844C>G	ENSP00000250087.5:p.Gln282Glu
ENST00000381128.2:c.*905C>G	ENSP00000370520.2:n.*905C>G
ENST00000381129.7:c.1033C>G	ENSP00000370521.3:p.Gln345Glu
ENST00000570466.5:c.967C>G	ENSP00000461287.1:p.Gln323Glu
ENST00000570584.5:c.251+8337C>G
ENST00000574506.5:c.997C>G	ENSP00000458456.1:p.Gln333Glu
ENST00000575265.5:c.*1004C>G	ENSP00000459673.1:n.*1004C>G
ENST00000576307.5:c.853C>G	ENSP00000459522.1:p.Gln285Glu
ENST00000576776.5:c.961C>G	ENSP00000460827.1:p.Gln321Glu
ENST00000621374.4:c.*51C>G	ENSP00000481337.1:n.*51C>G
NM_001033054.2:c.844C>G	NP_001028226.1:p.Gln282Glu
NM_001033055.2:c.853C>G	NP_001028227.1:p.Gln285Glu
NM_001285399.2:c.997C>G	NP_001272328.1:p.Gln333Glu
NM_001285400.2:c.967C>G	NP_001272329.1:p.Gln323Glu
NM_001285401.2:c.961C>G	NP_001272330.1:p.Gln321Glu
NM_001285402.1:c.916C>G	NP_001272331.1:p.Gln306Glu
NM_014336.4:c.1033C>G	NP_055151.3:p.Gln345Glu
NM_001033054.3:c.844C>G	NP_001028226.1:p.Gln282Glu
NM_001033055.3:c.853C>G	NP_001028227.1:p.Gln285Glu
NM_001285399.3:c.997C>G	NP_001272328.1:p.Gln333Glu
NM_001285400.3:c.967C>G	NP_001272329.1:p.Gln323Glu
NM_001285401.3:c.961C>G	NP_001272330.1:p.Gln321Glu
NM_001285402.2:c.916C>G	NP_001272331.1:p.Gln306Glu
NM_001285403.3:c.*1004C>G	NP_001272332.1:n.*1004C>G
NM_014336.5:c.1033C>G MANE Select	NP_055151.3:p.Gln345Glu
NM_001285403.4:c.*1004C>G	NP_001272332.1:n.*1004C>G