Canonical Allele Identifier: CA386296212

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155405C>G (hg19) ; chr12:g.101761627C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761627C>G , CM000674.2:g.101761627C>G	GRCh38
NC_000012.11:g.102155405C>G , CM000674.1:g.102155405C>G	GRCh37
NC_000012.10:g.100679536C>G	NCBI36
NG_021243.1:g.74241G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2852G>C MANE Select	ENSP00000299314.7:p.Arg951Pro
ENST00000299314.11:c.2852G>C	ENSP00000299314.7:p.Arg951Pro
NM_024312.4:c.2852G>C	NP_077288.2:p.Arg951Pro
XM_006719593.2:c.2852G>C	XP_006719656.1:p.Arg951Pro
XM_011538731.1:c.2771G>C	XP_011537033.1:p.Arg924Pro
XM_006719593.3:c.2852G>C	XP_006719656.1:p.Arg951Pro
XM_011538731.2:c.2771G>C	XP_011537033.1:p.Arg924Pro
XM_017019961.1:c.2636G>C	XP_016875450.1:p.Arg879Pro
XM_017019962.2:c.1625G>C	XP_016875451.1:p.Arg542Pro
NM_024312.5:c.2852G>C MANE Select	NP_077288.2:p.Arg951Pro