Canonical Allele Identifier: CA2058956990

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768120C= , CM000674.2:g.101768120C=	GRCh38
NC_000012.11:g.102161898C= , CM000674.1:g.102161898C=	GRCh37
NC_000012.10:g.100686029C=	NCBI36
NG_021243.1:g.67748G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1325G= MANE Select	ENSP00000299314.7:p.Cys442=
ENST00000299314.11:c.1325G=	ENSP00000299314.7:p.Cys442=
ENST00000549940.5:c.1325G=	ENSP00000449150.1:p.Cys442=
NM_024312.4:c.1325G=	NP_077288.2:p.Cys442=
XM_006719593.2:c.1325G=	XP_006719656.1:p.Cys442=
XM_011538731.1:c.1244G=	XP_011537033.1:p.Cys415=
XM_006719593.3:c.1325G=	XP_006719656.1:p.Cys442=
XM_011538731.2:c.1244G=	XP_011537033.1:p.Cys415=
XM_017019961.1:c.1109G=	XP_016875450.1:p.Cys370=
XM_017019962.2:c.98G=	XP_016875451.1:p.Cys33=
NM_024312.5:c.1325G= MANE Select	NP_077288.2:p.Cys442=