Canonical Allele Identifier: CA386292296
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3553C>G MANE Select ENSP00000299314.7:p.Pro1185Ala
ENST00000299314.11:c.3553C>G ENSP00000299314.7:p.Pro1185Ala
ENST00000549738.5:c.451C>G ENSP00000450161.1:n.451C>G
NM_024312.4:c.3553C>G NP_077288.2:p.Pro1185Ala
XM_011538731.1:c.3472C>G XP_011537033.1:p.Pro1158Ala
XM_011538731.2:c.3472C>G XP_011537033.1:p.Pro1158Ala
XM_017019961.1:c.3337C>G XP_016875450.1:p.Pro1113Ala
XM_017019962.2:c.2326C>G XP_016875451.1:p.Pro776Ala
NM_024312.5:c.3553C>G MANE Select NP_077288.2:p.Pro1185Ala