Canonical Allele Identifier: CA2058953290

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761773G= , CM000674.2:g.101761773G=	GRCh38
NC_000012.11:g.102155551G= , CM000674.1:g.102155551G=	GRCh37
NC_000012.10:g.100679682G=	NCBI36
NG_021243.1:g.74095C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2716-10C= MANE Select	ENSP00000299314.7:n.2716-10C=
ENST00000299314.11:c.2716-10C=	ENSP00000299314.7:n.2716-10C=
NM_024312.4:c.2716-10C=	NP_077288.2:n.2716-10C=
XM_006719593.2:c.2716-10C=	XP_006719656.1:n.2716-10C=
XM_011538731.1:c.2635-10C=	XP_011537033.1:n.2635-10C=
XM_006719593.3:c.2716-10C=	XP_006719656.1:n.2716-10C=
XM_011538731.2:c.2635-10C=	XP_011537033.1:n.2635-10C=
XM_017019961.1:c.2500-10C=	XP_016875450.1:n.2500-10C=
XM_017019962.2:c.1489-10C=	XP_016875451.1:n.1489-10C=
NM_024312.5:c.2716-10C= MANE Select	NP_077288.2:n.2716-10C=