Canonical Allele Identifier: CA397394843

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425787C>A , CM000679.2:g.6425787C>A	GRCh38
NC_000017.10:g.6329107C>A , CM000679.1:g.6329107C>A	GRCh37
NC_000017.9:g.6269831C>A	NCBI36
NG_008474.1:g.14413G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014336.5:c.828G>T MANE Select	NP_055151.3:p.Glu276Asp
ENST00000381129.8:c.828G>T MANE Select	ENSP00000370521.3:p.Glu276Asp
NM_001033054.2:c.639G>T	NP_001028226.1:p.Glu213Asp
NM_001033054.3:c.639G>T	NP_001028226.1:p.Glu213Asp
NM_001033055.2:c.648G>T	NP_001028227.1:p.Glu216Asp
NM_001033055.3:c.648G>T	NP_001028227.1:p.Glu216Asp
NM_001285399.2:c.792G>T	NP_001272328.1:p.Glu264Asp
NM_001285399.3:c.792G>T	NP_001272328.1:p.Glu264Asp
NM_001285400.2:c.762G>T	NP_001272329.1:p.Glu254Asp
NM_001285400.3:c.762G>T	NP_001272329.1:p.Glu254Asp
NM_001285401.2:c.756G>T	NP_001272330.1:p.Glu252Asp
NM_001285401.3:c.756G>T	NP_001272330.1:p.Glu252Asp
NM_001285402.1:c.711G>T	NP_001272331.1:p.Glu237Asp
NM_001285402.2:c.711G>T	NP_001272331.1:p.Glu237Asp
NM_001285403.3:c.*799G>T	NP_001272332.1:n.*799G>T
NM_001285403.4:c.*799G>T	NP_001272332.1:n.*799G>T
NM_014336.4:c.828G>T	NP_055151.3:p.Glu276Asp
ENST00000250087.9:c.639G>T	ENSP00000250087.5:p.Glu213Asp
ENST00000381128.2:c.*700G>T	ENSP00000370520.2:n.*700G>T
ENST00000381129.7:c.828G>T	ENSP00000370521.3:p.Glu276Asp
ENST00000570466.5:c.762G>T	ENSP00000461287.1:p.Glu254Asp
ENST00000570584.5:c.251+8132G>T
ENST00000574506.5:c.792G>T	ENSP00000458456.1:p.Glu264Asp
ENST00000575265.5:c.*799G>T	ENSP00000459673.1:n.*799G>T
ENST00000576307.5:c.648G>T	ENSP00000459522.1:p.Glu216Asp
ENST00000576776.5:c.756G>T	ENSP00000460827.1:p.Glu252Asp
ENST00000621374.4:c.828G>T	ENSP00000481337.1:p.Glu276Asp