Canonical Allele Identifier: CA386302008
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101768124C>G , CM000674.2:g.101768124C>G GRCh38
NC_000012.11:g.102161902C>G , CM000674.1:g.102161902C>G GRCh37
NC_000012.10:g.100686033C>G NCBI36
NG_021243.1:g.67744G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.1321G>C MANE Select ENSP00000299314.7:p.Gly441Arg
ENST00000299314.11:c.1321G>C ENSP00000299314.7:p.Gly441Arg
ENST00000549940.5:c.1321G>C ENSP00000449150.1:p.Gly441Arg
NM_024312.4:c.1321G>C NP_077288.2:p.Gly441Arg
XM_006719593.2:c.1321G>C XP_006719656.1:p.Gly441Arg
XM_011538731.1:c.1240G>C XP_011537033.1:p.Gly414Arg
XM_006719593.3:c.1321G>C XP_006719656.1:p.Gly441Arg
XM_011538731.2:c.1240G>C XP_011537033.1:p.Gly414Arg
XM_017019961.1:c.1105G>C XP_016875450.1:p.Gly369Arg
XM_017019962.2:c.94G>C XP_016875451.1:p.Gly32Arg
NM_024312.5:c.1321G>C MANE Select NP_077288.2:p.Gly441Arg