Canonical Allele Identifier: CA2058953155

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761692A= , CM000674.2:g.101761692A=	GRCh38
NC_000012.11:g.102155470A= , CM000674.1:g.102155470A=	GRCh37
NC_000012.10:g.100679601A=	NCBI36
NG_021243.1:g.74176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2787T= MANE Select	ENSP00000299314.7:p.Asp929=
ENST00000299314.11:c.2787T=	ENSP00000299314.7:p.Asp929=
NM_024312.4:c.2787T=	NP_077288.2:p.Asp929=
XM_006719593.2:c.2787T=	XP_006719656.1:p.Asp929=
XM_011538731.1:c.2706T=	XP_011537033.1:p.Asp902=
XM_006719593.3:c.2787T=	XP_006719656.1:p.Asp929=
XM_011538731.2:c.2706T=	XP_011537033.1:p.Asp902=
XM_017019961.1:c.2571T=	XP_016875450.1:p.Asp857=
XM_017019962.2:c.1560T=	XP_016875451.1:p.Asp520=
NM_024312.5:c.2787T= MANE Select	NP_077288.2:p.Asp929=