Canonical Allele Identifier: CA397394210

Gene: AIPL1

Linked Data

• dbSNP Id: rs1333977042
• gnomAD v2: 17-6328808-G-A
• gnomAD v3: 17-6425488-G-A
• gnomAD v4: 17-6425488-G-A
• MyVariant Identifiers: chr17:g.6328808G>A (hg19) ; chr17:g.6425488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425488G>A , CM000679.2:g.6425488G>A	GRCh38
NC_000017.10:g.6328808G>A , CM000679.1:g.6328808G>A	GRCh37
NC_000017.9:g.6269532G>A	NCBI36
NG_008474.1:g.14712C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1127C>T MANE Select	ENSP00000370521.3:p.Pro376Leu
ENST00000250087.9:c.938C>T	ENSP00000250087.5:p.Pro313Leu
ENST00000381128.2:c.*999C>T	ENSP00000370520.2:n.*999C>T
ENST00000381129.7:c.1127C>T	ENSP00000370521.3:p.Pro376Leu
ENST00000570466.5:c.1061C>T	ENSP00000461287.1:p.Pro354Leu
ENST00000570584.5:c.251+8431C>T
ENST00000574506.5:c.1091C>T	ENSP00000458456.1:p.Pro364Leu
ENST00000575265.5:c.*1098C>T	ENSP00000459673.1:n.*1098C>T
ENST00000576307.5:c.947C>T	ENSP00000459522.1:p.Pro316Leu
ENST00000576776.5:c.1055C>T	ENSP00000460827.1:p.Pro352Leu
ENST00000621374.4:c.*145C>T	ENSP00000481337.1:n.*145C>T
NM_001033054.2:c.938C>T	NP_001028226.1:p.Pro313Leu
NM_001033055.2:c.947C>T	NP_001028227.1:p.Pro316Leu
NM_001285399.2:c.1091C>T	NP_001272328.1:p.Pro364Leu
NM_001285400.2:c.1061C>T	NP_001272329.1:p.Pro354Leu
NM_001285401.2:c.1055C>T	NP_001272330.1:p.Pro352Leu
NM_001285402.1:c.1010C>T	NP_001272331.1:p.Pro337Leu
NM_014336.4:c.1127C>T	NP_055151.3:p.Pro376Leu
NM_001033054.3:c.938C>T	NP_001028226.1:p.Pro313Leu
NM_001033055.3:c.947C>T	NP_001028227.1:p.Pro316Leu
NM_001285399.3:c.1091C>T	NP_001272328.1:p.Pro364Leu
NM_001285400.3:c.1061C>T	NP_001272329.1:p.Pro354Leu
NM_001285401.3:c.1055C>T	NP_001272330.1:p.Pro352Leu
NM_001285402.2:c.1010C>T	NP_001272331.1:p.Pro337Leu
NM_001285403.3:c.*1098C>T	NP_001272332.1:n.*1098C>T
NM_014336.5:c.1127C>T MANE Select	NP_055151.3:p.Pro376Leu
NM_001285403.4:c.*1098C>T	NP_001272332.1:n.*1098C>T