Canonical Allele Identifier: CA386301736

Gene: GNPTAB

Linked Data

• dbSNP Id: rs1953120485
• MyVariant Identifiers: chr12:g.102161824C>G (hg19) ; chr12:g.101768046C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768046C>G , CM000674.2:g.101768046C>G	GRCh38
NC_000012.11:g.102161824C>G , CM000674.1:g.102161824C>G	GRCh37
NC_000012.10:g.100685955C>G	NCBI36
NG_021243.1:g.67822G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1399G>C MANE Select	ENSP00000299314.7:p.Asp467His
ENST00000299314.11:c.1399G>C	ENSP00000299314.7:p.Asp467His
ENST00000549940.5:c.1399G>C	ENSP00000449150.1:p.Asp467His
ENST00000552009.1:n.58G>C
NM_024312.4:c.1399G>C	NP_077288.2:p.Asp467His
XM_006719593.2:c.1399G>C	XP_006719656.1:p.Asp467His
XM_011538731.1:c.1318G>C	XP_011537033.1:p.Asp440His
XM_006719593.3:c.1399G>C	XP_006719656.1:p.Asp467His
XM_011538731.2:c.1318G>C	XP_011537033.1:p.Asp440His
XM_017019961.1:c.1183G>C	XP_016875450.1:p.Asp395His
XM_017019962.2:c.172G>C	XP_016875451.1:p.Asp58His
NM_024312.5:c.1399G>C MANE Select	NP_077288.2:p.Asp467His