Canonical Allele Identifier: CA2058958096

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770721A= , CM000674.2:g.101770721A=	GRCh38
NC_000012.11:g.102164499A= , CM000674.1:g.102164499A=	GRCh37
NC_000012.10:g.100688630A=	NCBI36
NG_021243.1:g.65147T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.934-136T= MANE Select	ENSP00000299314.7:n.934-136T=
ENST00000299314.11:c.934-136T=	ENSP00000299314.7:n.934-136T=
ENST00000549940.5:c.934-136T=	ENSP00000449150.1:n.934-136T=
NM_024312.4:c.934-136T=	NP_077288.2:n.934-136T=
XM_006719593.2:c.934-136T=	XP_006719656.1:n.934-136T=
XM_011538731.1:c.853-136T=	XP_011537033.1:n.853-136T=
XM_006719593.3:c.934-136T=	XP_006719656.1:n.934-136T=
XM_011538731.2:c.853-136T=	XP_011537033.1:n.853-136T=
XM_017019961.1:c.718-136T=	XP_016875450.1:n.718-136T=
XM_017019962.2:c.-417-13T=	XP_016875451.1:n.-417-13T=
NM_024312.5:c.934-136T= MANE Select	NP_077288.2:n.934-136T=