Canonical Allele Identifier: CA475195756
Gene: GAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68453106G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68685638G>A , CM000673.2:g.68685638G>A GRCh38
NC_000011.9:g.68453106G>A , CM000673.1:g.68453106G>A GRCh37
NC_000011.8:g.68209682G>A NCBI36
NG_052785.1:g.6164G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265643.4:c.126G>A MANE Select ENSP00000265643.3:p.Leu42=
ENST00000265643.3:c.126G>A ENSP00000265643.3:p.Leu42=
NM_015973.3:c.126G>A NP_057057.2:p.Leu42=
NM_015973.4:c.126G>A NP_057057.2:p.Leu42=
XR_001748281.1:n.230+2203C>T
NM_015973.5:c.126G>A MANE Select NP_057057.2:p.Leu42=