Canonical Allele Identifier: CA2058950507
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753324T= , CM000674.2:g.101753324T= GRCh38
NC_000012.11:g.102147102T= , CM000674.1:g.102147102T= GRCh37
NC_000012.10:g.100671233T= NCBI36
NG_021243.1:g.82544A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3602+48A= MANE Select ENSP00000299314.7:n.3602+48A=
ENST00000299314.11:c.3602+48A= ENSP00000299314.7:n.3602+48A=
ENST00000549738.5:c.500+48A= ENSP00000450161.1:n.500+48A=
NM_024312.4:c.3602+48A= NP_077288.2:n.3602+48A=
XM_011538731.1:c.3521+48A= XP_011537033.1:n.3521+48A=
XM_011538731.2:c.3521+48A= XP_011537033.1:n.3521+48A=
XM_017019961.1:c.3386+48A= XP_016875450.1:n.3386+48A=
XM_017019962.2:c.2375+48A= XP_016875451.1:n.2375+48A=
NM_024312.5:c.3602+48A= MANE Select NP_077288.2:n.3602+48A=