Canonical Allele Identifier: CA8328302

Gene: AIPL1

Linked Data

• dbSNP Id: rs756123820
• ExAC: 17:6328792 C / A
• gnomAD v2: 17-6328792-C-A
• gnomAD v3: 17-6425472-C-A
• gnomAD v4: 17-6425472-C-A
• MyVariant Identifiers: chr17:g.6328792C>A (hg19) ; chr17:g.6425472C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425472C>A , CM000679.2:g.6425472C>A	GRCh38
NC_000017.10:g.6328792C>A , CM000679.1:g.6328792C>A	GRCh37
NC_000017.9:g.6269516C>A	NCBI36
NG_008474.1:g.14728G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1143G>T MANE Select	ENSP00000370521.3:p.Ser381=
ENST00000250087.9:c.954G>T	ENSP00000250087.5:p.Ser318=
ENST00000381128.2:c.*1015G>T	ENSP00000370520.2:n.*1015G>T
ENST00000381129.7:c.1143G>T	ENSP00000370521.3:p.Ser381=
ENST00000570466.5:c.1077G>T	ENSP00000461287.1:p.Ser359=
ENST00000570584.5:c.251+8447G>T
ENST00000574506.5:c.1107G>T	ENSP00000458456.1:p.Ser369=
ENST00000575265.5:c.*1114G>T	ENSP00000459673.1:n.*1114G>T
ENST00000576307.5:c.963G>T	ENSP00000459522.1:p.Ser321=
ENST00000576776.5:c.1071G>T	ENSP00000460827.1:p.Ser357=
ENST00000621374.4:c.*161G>T	ENSP00000481337.1:n.*161G>T
NM_001033054.2:c.954G>T	NP_001028226.1:p.Ser318=
NM_001033055.2:c.963G>T	NP_001028227.1:p.Ser321=
NM_001285399.2:c.1107G>T	NP_001272328.1:p.Ser369=
NM_001285400.2:c.1077G>T	NP_001272329.1:p.Ser359=
NM_001285401.2:c.1071G>T	NP_001272330.1:p.Ser357=
NM_001285402.1:c.1026G>T	NP_001272331.1:p.Ser342=
NM_014336.4:c.1143G>T	NP_055151.3:p.Ser381=
NM_001033054.3:c.954G>T	NP_001028226.1:p.Ser318=
NM_001033055.3:c.963G>T	NP_001028227.1:p.Ser321=
NM_001285399.3:c.1107G>T	NP_001272328.1:p.Ser369=
NM_001285400.3:c.1077G>T	NP_001272329.1:p.Ser359=
NM_001285401.3:c.1071G>T	NP_001272330.1:p.Ser357=
NM_001285402.2:c.1026G>T	NP_001272331.1:p.Ser342=
NM_001285403.3:c.*1114G>T	NP_001272332.1:n.*1114G>T
NM_014336.5:c.1143G>T MANE Select	NP_055151.3:p.Ser381=
NM_001285403.4:c.*1114G>T	NP_001272332.1:n.*1114G>T