Canonical Allele Identifier: CA397394512

Gene: AIPL1

Linked Data

• dbSNP Id: rs2150674330
• MyVariant Identifiers: chr17:g.6328960G>A (hg19) ; chr17:g.6425640G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425640G>A , CM000679.2:g.6425640G>A	GRCh38
NC_000017.10:g.6328960G>A , CM000679.1:g.6328960G>A	GRCh37
NC_000017.9:g.6269684G>A	NCBI36
NG_008474.1:g.14560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.975C>T MANE Select	ENSP00000370521.3:p.Asn325=
ENST00000250087.9:c.786C>T	ENSP00000250087.5:p.Asn262=
ENST00000381128.2:c.*847C>T	ENSP00000370520.2:n.*847C>T
ENST00000381129.7:c.975C>T	ENSP00000370521.3:p.Asn325=
ENST00000570466.5:c.909C>T	ENSP00000461287.1:p.Asn303=
ENST00000570584.5:c.251+8279C>T
ENST00000574506.5:c.939C>T	ENSP00000458456.1:p.Asn313=
ENST00000575265.5:c.*946C>T	ENSP00000459673.1:n.*946C>T
ENST00000576307.5:c.795C>T	ENSP00000459522.1:p.Asn265=
ENST00000576776.5:c.903C>T	ENSP00000460827.1:p.Asn301=
ENST00000621374.4:c.974C>T	ENSP00000481337.1:p.Thr325Ile
NM_001033054.2:c.786C>T	NP_001028226.1:p.Asn262=
NM_001033055.2:c.795C>T	NP_001028227.1:p.Asn265=
NM_001285399.2:c.939C>T	NP_001272328.1:p.Asn313=
NM_001285400.2:c.909C>T	NP_001272329.1:p.Asn303=
NM_001285401.2:c.903C>T	NP_001272330.1:p.Asn301=
NM_001285402.1:c.858C>T	NP_001272331.1:p.Asn286=
NM_014336.4:c.975C>T	NP_055151.3:p.Asn325=
NM_001033054.3:c.786C>T	NP_001028226.1:p.Asn262=
NM_001033055.3:c.795C>T	NP_001028227.1:p.Asn265=
NM_001285399.3:c.939C>T	NP_001272328.1:p.Asn313=
NM_001285400.3:c.909C>T	NP_001272329.1:p.Asn303=
NM_001285401.3:c.903C>T	NP_001272330.1:p.Asn301=
NM_001285402.2:c.858C>T	NP_001272331.1:p.Asn286=
NM_001285403.3:c.*946C>T	NP_001272332.1:n.*946C>T
NM_014336.5:c.975C>T MANE Select	NP_055151.3:p.Asn325=
NM_001285403.4:c.*946C>T	NP_001272332.1:n.*946C>T