Canonical Allele Identifier: CA2058964711

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101785826T= , CM000674.2:g.101785826T=	GRCh38
NC_000012.11:g.102179604T= , CM000674.1:g.102179604T=	GRCh37
NC_000012.10:g.100703735T=	NCBI36
NG_021243.1:g.50042A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.571+186A= MANE Select	ENSP00000299314.7:n.571+186A=
ENST00000299314.11:c.571+186A=	ENSP00000299314.7:n.571+186A=
ENST00000549940.5:c.571+186A=	ENSP00000449150.1:n.571+186A=
ENST00000550352.1:n.551A=
ENST00000552681.1:c.205+186A=	ENSP00000449217.1:n.205+186A=
NM_024312.4:c.571+186A=	NP_077288.2:n.571+186A=
XM_006719593.2:c.571+186A=	XP_006719656.1:n.571+186A=
XM_011538731.1:c.490+186A=	XP_011537033.1:n.490+186A=
XM_006719593.3:c.571+186A=	XP_006719656.1:n.571+186A=
XM_011538731.2:c.490+186A=	XP_011537033.1:n.490+186A=
XM_017019961.1:c.355+186A=	XP_016875450.1:n.355+186A=
XM_017019962.2:c.-780+186A=	XP_016875451.1:n.-780+186A=
NM_024312.5:c.571+186A= MANE Select	NP_077288.2:n.571+186A=