Canonical Allele Identifier: CA397394168

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425465-G-T
• MyVariant Identifiers: chr17:g.6328785G>T (hg19) ; chr17:g.6425465G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425465G>T , CM000679.2:g.6425465G>T	GRCh38
NC_000017.10:g.6328785G>T , CM000679.1:g.6328785G>T	GRCh37
NC_000017.9:g.6269509G>T	NCBI36
NG_008474.1:g.14735C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1150C>A MANE Select	ENSP00000370521.3:p.His384Asn
ENST00000250087.9:c.961C>A	ENSP00000250087.5:p.His321Asn
ENST00000381128.2:c.*1022C>A	ENSP00000370520.2:n.*1022C>A
ENST00000381129.7:c.1150C>A	ENSP00000370521.3:p.His384Asn
ENST00000570466.5:c.1084C>A	ENSP00000461287.1:p.His362Asn
ENST00000570584.5:c.251+8454C>A
ENST00000574506.5:c.1114C>A	ENSP00000458456.1:p.His372Asn
ENST00000575265.5:c.*1121C>A	ENSP00000459673.1:n.*1121C>A
ENST00000576307.5:c.970C>A	ENSP00000459522.1:p.His324Asn
ENST00000576776.5:c.1078C>A	ENSP00000460827.1:p.His360Asn
ENST00000621374.4:c.*168C>A	ENSP00000481337.1:n.*168C>A
NM_001033054.2:c.961C>A	NP_001028226.1:p.His321Asn
NM_001033055.2:c.970C>A	NP_001028227.1:p.His324Asn
NM_001285399.2:c.1114C>A	NP_001272328.1:p.His372Asn
NM_001285400.2:c.1084C>A	NP_001272329.1:p.His362Asn
NM_001285401.2:c.1078C>A	NP_001272330.1:p.His360Asn
NM_001285402.1:c.1033C>A	NP_001272331.1:p.His345Asn
NM_014336.4:c.1150C>A	NP_055151.3:p.His384Asn
NM_001033054.3:c.961C>A	NP_001028226.1:p.His321Asn
NM_001033055.3:c.970C>A	NP_001028227.1:p.His324Asn
NM_001285399.3:c.1114C>A	NP_001272328.1:p.His372Asn
NM_001285400.3:c.1084C>A	NP_001272329.1:p.His362Asn
NM_001285401.3:c.1078C>A	NP_001272330.1:p.His360Asn
NM_001285402.2:c.1033C>A	NP_001272331.1:p.His345Asn
NM_001285403.3:c.*1121C>A	NP_001272332.1:n.*1121C>A
NM_014336.5:c.1150C>A MANE Select	NP_055151.3:p.His384Asn
NM_001285403.4:c.*1121C>A	NP_001272332.1:n.*1121C>A