Canonical Allele Identifier: CA2058964844

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786145T= , CM000674.2:g.101786145T=	GRCh38
NC_000012.11:g.102179923T= , CM000674.1:g.102179923T=	GRCh37
NC_000012.10:g.100704054T=	NCBI36
NG_021243.1:g.49723A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.438A= MANE Select	ENSP00000299314.7:p.Pro146=
ENST00000299314.11:c.438A=	ENSP00000299314.7:p.Pro146=
ENST00000549940.5:c.438A=	ENSP00000449150.1:p.Pro146=
ENST00000550352.1:n.232A=
ENST00000552681.1:c.72A=	ENSP00000449217.1:p.Pro24=
NM_024312.4:c.438A=	NP_077288.2:p.Pro146=
XM_006719593.2:c.438A=	XP_006719656.1:p.Pro146=
XM_011538731.1:c.357A=	XP_011537033.1:p.Pro119=
XM_006719593.3:c.438A=	XP_006719656.1:p.Pro146=
XM_011538731.2:c.357A=	XP_011537033.1:p.Pro119=
XM_017019961.1:c.222A=	XP_016875450.1:p.Pro74=
XM_017019962.2:c.-913A=	XP_016875451.1:n.-913A=
NM_024312.5:c.438A= MANE Select	NP_077288.2:p.Pro146=