Canonical Allele Identifier: CA386292279
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753417C>T , CM000674.2:g.101753417C>T GRCh38
NC_000012.11:g.102147195C>T , CM000674.1:g.102147195C>T GRCh37
NC_000012.10:g.100671326C>T NCBI36
NG_021243.1:g.82451G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3557G>A MANE Select ENSP00000299314.7:p.Arg1186Lys
ENST00000299314.11:c.3557G>A ENSP00000299314.7:p.Arg1186Lys
ENST00000549738.5:c.455G>A ENSP00000450161.1:n.455G>A
NM_024312.4:c.3557G>A NP_077288.2:p.Arg1186Lys
XM_011538731.1:c.3476G>A XP_011537033.1:p.Arg1159Lys
XM_011538731.2:c.3476G>A XP_011537033.1:p.Arg1159Lys
XM_017019961.1:c.3341G>A XP_016875450.1:p.Arg1114Lys
XM_017019962.2:c.2330G>A XP_016875451.1:p.Arg777Lys
NM_024312.5:c.3557G>A MANE Select NP_077288.2:p.Arg1186Lys