Canonical Allele Identifier: CA2058969456

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796730A= , CM000674.2:g.101796730A=	GRCh38
NC_000012.11:g.102190508A= , CM000674.1:g.102190508A=	GRCh37
NC_000012.10:g.100714639A=	NCBI36
NG_021243.1:g.39138T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.150T= MANE Select	ENSP00000299314.7:p.His50=
ENST00000647144.1:n.270T=
ENST00000299314.11:c.150T=	ENSP00000299314.7:p.His50=
ENST00000392919.4:c.150T=	ENSP00000376651.4:p.His50=
ENST00000549165.1:c.150T=	ENSP00000450413.1:p.His50=
ENST00000549940.5:c.150T=	ENSP00000449150.1:p.His50=
NM_024312.4:c.150T=	NP_077288.2:p.His50=
XM_006719593.2:c.150T=	XP_006719656.1:p.His50=
XM_011538731.1:c.69T=	XP_011537033.1:p.His23=
XM_006719593.3:c.150T=	XP_006719656.1:p.His50=
XM_011538731.2:c.69T=	XP_011537033.1:p.His23=
XM_017019961.1:c.-67T=	XP_016875450.1:n.-67T=
XM_017019962.2:c.-1201T=	XP_016875451.1:n.-1201T=
NM_024312.5:c.150T= MANE Select	NP_077288.2:p.His50=