Canonical Allele Identifier: CA2058964833

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786124G= , CM000674.2:g.101786124G=	GRCh38
NC_000012.11:g.102179902G= , CM000674.1:g.102179902G=	GRCh37
NC_000012.10:g.100704033G=	NCBI36
NG_021243.1:g.49744C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.459C= MANE Select	ENSP00000299314.7:p.Asp153=
ENST00000299314.11:c.459C=	ENSP00000299314.7:p.Asp153=
ENST00000549940.5:c.459C=	ENSP00000449150.1:p.Asp153=
ENST00000550352.1:n.253C=
ENST00000552681.1:c.93C=	ENSP00000449217.1:p.Asp31=
NM_024312.4:c.459C=	NP_077288.2:p.Asp153=
XM_006719593.2:c.459C=	XP_006719656.1:p.Asp153=
XM_011538731.1:c.378C=	XP_011537033.1:p.Asp126=
XM_006719593.3:c.459C=	XP_006719656.1:p.Asp153=
XM_011538731.2:c.378C=	XP_011537033.1:p.Asp126=
XM_017019961.1:c.243C=	XP_016875450.1:p.Asp81=
XM_017019962.2:c.-892C=	XP_016875451.1:n.-892C=
NM_024312.5:c.459C= MANE Select	NP_077288.2:p.Asp153=