Canonical Allele Identifier: CA2058964801

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786064T= , CM000674.2:g.101786064T=	GRCh38
NC_000012.11:g.102179842T= , CM000674.1:g.102179842T=	GRCh37
NC_000012.10:g.100703973T=	NCBI36
NG_021243.1:g.49804A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.519A= MANE Select	ENSP00000299314.7:p.Pro173=
ENST00000299314.11:c.519A=	ENSP00000299314.7:p.Pro173=
ENST00000549940.5:c.519A=	ENSP00000449150.1:p.Pro173=
ENST00000550352.1:n.313A=
ENST00000552681.1:c.153A=	ENSP00000449217.1:p.Pro51=
NM_024312.4:c.519A=	NP_077288.2:p.Pro173=
XM_006719593.2:c.519A=	XP_006719656.1:p.Pro173=
XM_011538731.1:c.438A=	XP_011537033.1:p.Pro146=
XM_006719593.3:c.519A=	XP_006719656.1:p.Pro173=
XM_011538731.2:c.438A=	XP_011537033.1:p.Pro146=
XM_017019961.1:c.303A=	XP_016875450.1:p.Pro101=
XM_017019962.2:c.-832A=	XP_016875451.1:n.-832A=
NM_024312.5:c.519A= MANE Select	NP_077288.2:p.Pro173=