Canonical Allele Identifier: CA386292294
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753421G>A , CM000674.2:g.101753421G>A GRCh38
NC_000012.11:g.102147199G>A , CM000674.1:g.102147199G>A GRCh37
NC_000012.10:g.100671330G>A NCBI36
NG_021243.1:g.82447C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3553C>T MANE Select ENSP00000299314.7:p.Pro1185Ser
ENST00000299314.11:c.3553C>T ENSP00000299314.7:p.Pro1185Ser
ENST00000549738.5:c.451C>T ENSP00000450161.1:n.451C>T
NM_024312.4:c.3553C>T NP_077288.2:p.Pro1185Ser
XM_011538731.1:c.3472C>T XP_011537033.1:p.Pro1158Ser
XM_011538731.2:c.3472C>T XP_011537033.1:p.Pro1158Ser
XM_017019961.1:c.3337C>T XP_016875450.1:p.Pro1113Ser
XM_017019962.2:c.2326C>T XP_016875451.1:p.Pro776Ser
NM_024312.5:c.3553C>T MANE Select NP_077288.2:p.Pro1185Ser