Canonical Allele Identifier: CA2058964835

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786126C= , CM000674.2:g.101786126C=	GRCh38
NC_000012.11:g.102179904C= , CM000674.1:g.102179904C=	GRCh37
NC_000012.10:g.100704035C=	NCBI36
NG_021243.1:g.49742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.457G= MANE Select	ENSP00000299314.7:p.Asp153=
ENST00000299314.11:c.457G=	ENSP00000299314.7:p.Asp153=
ENST00000549940.5:c.457G=	ENSP00000449150.1:p.Asp153=
ENST00000550352.1:n.251G=
ENST00000552681.1:c.91G=	ENSP00000449217.1:p.Asp31=
NM_024312.4:c.457G=	NP_077288.2:p.Asp153=
XM_006719593.2:c.457G=	XP_006719656.1:p.Asp153=
XM_011538731.1:c.376G=	XP_011537033.1:p.Asp126=
XM_006719593.3:c.457G=	XP_006719656.1:p.Asp153=
XM_011538731.2:c.376G=	XP_011537033.1:p.Asp126=
XM_017019961.1:c.241G=	XP_016875450.1:p.Asp81=
XM_017019962.2:c.-894G=	XP_016875451.1:n.-894G=
NM_024312.5:c.457G= MANE Select	NP_077288.2:p.Asp153=