Canonical Allele Identifier: CA2579370995
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646611A>T , CM000671.2:g.34646611A>T GRCh38
NC_000009.11:g.34646608A>T , CM000671.1:g.34646608A>T GRCh37
NC_000009.10:g.34636608A>T NCBI36
NG_009029.1:g.4974A>T
NG_009029.2:g.5023A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-296A>T ENSP00000401956.2:n.-296A>T
ENST00000605275.1:n.209-66A>T
NM_000155.3:c.-94A>T NP_000146.2:n.-94A>T
NM_001258332.1:c.-296A>T NP_001245261.1:n.-296A>T