Canonical Allele Identifier: CA2841179358
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646607A>G , CM000671.2:g.34646607A>G GRCh38
NC_000009.11:g.34646604A>G , CM000671.1:g.34646604A>G GRCh37
NC_000009.10:g.34636604A>G NCBI36
NG_009029.1:g.4970A>G
NG_009029.2:g.5019A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000450095.6:c.-300A>G ENSP00000401956.2:n.-300A>G
ENST00000605275.1:n.209-70A>G
NM_000155.3:c.-98A>G NP_000146.2:n.-98A>G
NM_001258332.1:c.-300A>G NP_001245261.1:n.-300A>G