Canonical Allele Identifier: CA2058952491

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761223G= , CM000674.2:g.101761223G=	GRCh38
NC_000012.11:g.102155001G= , CM000674.1:g.102155001G=	GRCh37
NC_000012.10:g.100679132G=	NCBI36
NG_021243.1:g.74645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3039C= MANE Select	ENSP00000299314.7:p.Val1013=
ENST00000299314.11:c.3039C=	ENSP00000299314.7:p.Val1013=
NM_024312.4:c.3039C=	NP_077288.2:p.Val1013=
XM_006719593.2:c.3039C=	XP_006719656.1:p.Val1013=
XM_011538731.1:c.2958C=	XP_011537033.1:p.Val986=
XM_006719593.3:c.3039C=	XP_006719656.1:p.Val1013=
XM_011538731.2:c.2958C=	XP_011537033.1:p.Val986=
XM_017019961.1:c.2823C=	XP_016875450.1:p.Val941=
XM_017019962.2:c.1812C=	XP_016875451.1:p.Val604=
NM_024312.5:c.3039C= MANE Select	NP_077288.2:p.Val1013=