Canonical Allele Identifier: CA386486996
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830621C>G , CM000674.2:g.101830621C>G GRCh38
NC_000012.11:g.102224399C>G , CM000674.1:g.102224399C>G GRCh37
NC_000012.10:g.100748530C>G NCBI36
NG_021243.1:g.5247G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.55G>C MANE Select ENSP00000299314.7:p.Gly19Arg
ENST00000647144.1:n.43G>C
ENST00000299314.11:c.55G>C ENSP00000299314.7:p.Gly19Arg
ENST00000392919.4:c.55G>C ENSP00000376651.4:p.Gly19Arg
ENST00000549165.1:c.55G>C ENSP00000450413.1:p.Gly19Arg
ENST00000549940.5:c.55G>C ENSP00000449150.1:p.Gly19Arg
NM_024312.4:c.55G>C NP_077288.2:p.Gly19Arg
XM_006719593.2:c.55G>C XP_006719656.1:p.Gly19Arg
XM_006719593.3:c.55G>C XP_006719656.1:p.Gly19Arg
XM_017019961.1:c.-100+5G>C XP_016875450.1:n.-100+5G>C
XM_017019962.2:c.-1296G>C XP_016875451.1:n.-1296G>C
NM_024312.5:c.55G>C MANE Select NP_077288.2:p.Gly19Arg