Canonical Allele Identifier: CA386299250

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102158708C>G (hg19) ; chr12:g.101764930C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101764930C>G , CM000674.2:g.101764930C>G	GRCh38
NC_000012.11:g.102158708C>G , CM000674.1:g.102158708C>G	GRCh37
NC_000012.10:g.100682839C>G	NCBI36
NG_021243.1:g.70938G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1987G>C MANE Select	ENSP00000299314.7:p.Glu663Gln
ENST00000299314.11:c.1987G>C	ENSP00000299314.7:p.Glu663Gln
NM_024312.4:c.1987G>C	NP_077288.2:p.Glu663Gln
XM_006719593.2:c.1987G>C	XP_006719656.1:p.Glu663Gln
XM_011538731.1:c.1906G>C	XP_011537033.1:p.Glu636Gln
XM_006719593.3:c.1987G>C	XP_006719656.1:p.Glu663Gln
XM_011538731.2:c.1906G>C	XP_011537033.1:p.Glu636Gln
XM_017019961.1:c.1771G>C	XP_016875450.1:p.Glu591Gln
XM_017019962.2:c.760G>C	XP_016875451.1:p.Glu254Gln
NM_024312.5:c.1987G>C MANE Select	NP_077288.2:p.Glu663Gln