Canonical Allele Identifier: CA2058958011

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770503T= , CM000674.2:g.101770503T=	GRCh38
NC_000012.11:g.102164281T= , CM000674.1:g.102164281T=	GRCh37
NC_000012.10:g.100688412T=	NCBI36
NG_021243.1:g.65365A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1016A= MANE Select	ENSP00000299314.7:p.His339=
ENST00000299314.11:c.1016A=	ENSP00000299314.7:p.His339=
ENST00000549940.5:c.1016A=	ENSP00000449150.1:p.His339=
NM_024312.4:c.1016A=	NP_077288.2:p.His339=
XM_006719593.2:c.1016A=	XP_006719656.1:p.His339=
XM_011538731.1:c.935A=	XP_011537033.1:p.His312=
XM_006719593.3:c.1016A=	XP_006719656.1:p.His339=
XM_011538731.2:c.935A=	XP_011537033.1:p.His312=
XM_017019961.1:c.800A=	XP_016875450.1:p.His267=
XM_017019962.2:c.-212A=	XP_016875451.1:n.-212A=
NM_024312.5:c.1016A= MANE Select	NP_077288.2:p.His339=