Canonical Allele Identifier: CA381632905
Gene: GAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68685642G>A , CM000673.2:g.68685642G>A GRCh38
NC_000011.9:g.68453110G>A , CM000673.1:g.68453110G>A GRCh37
NC_000011.8:g.68209686G>A NCBI36
NG_052785.1:g.6168G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265643.4:c.130G>A MANE Select ENSP00000265643.3:p.Gly44Ser
ENST00000265643.3:c.130G>A ENSP00000265643.3:p.Gly44Ser
NM_015973.3:c.130G>A NP_057057.2:p.Gly44Ser
NM_015973.4:c.130G>A NP_057057.2:p.Gly44Ser
XR_001748281.1:n.230+2199C>T
NM_015973.5:c.130G>A MANE Select NP_057057.2:p.Gly44Ser