Canonical Allele Identifier: CA2614727617

Gene: GAL

Linked Data

• gnomAD v4: 11-68685469-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68685469G>T , CM000673.2:g.68685469G>T	GRCh38
NC_000011.9:g.68452937G>T , CM000673.1:g.68452937G>T	GRCh37
NC_000011.8:g.68209513G>T	NCBI36
NG_052785.1:g.5995G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265643.4:c.82-125G>T MANE Select	ENSP00000265643.3:n.82-125G>T
ENST00000265643.3:c.82-125G>T	ENSP00000265643.3:n.82-125G>T
NM_015973.3:c.82-125G>T	NP_057057.2:n.82-125G>T
NM_015973.4:c.82-125G>T	NP_057057.2:n.82-125G>T
XR_001748281.1:n.230+2372C>A
NM_015973.5:c.82-125G>T MANE Select	NP_057057.2:n.82-125G>T