Canonical Allele Identifier: CA373278701
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647194A>C , CM000671.2:g.34647194A>C GRCh38
NC_000009.11:g.34647191A>C , CM000671.1:g.34647191A>C GRCh37
NC_000009.10:g.34637191A>C NCBI36
NG_009029.1:g.5557A>C
NG_028966.1:g.10A>C
NG_009029.2:g.5606A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.188A>C ENSP00000509954.1:p.Lys63Thr
ENST00000378842.8:c.188A>C MANE Select ENSP00000368119.4:p.Lys63Thr
ENST00000378842.7:c.188A>C ENSP00000368119.3:p.Lys63Thr
ENST00000450095.6:c.-15A>C ENSP00000401956.2:n.-15A>C
ENST00000465543.6:n.527A>C
ENST00000468099.2:n.228A>C
ENST00000472111.5:n.229A>C
ENST00000473506.6:c.188A>C ENSP00000432839.2:p.Lys63Thr
ENST00000473529.5:n.235A>C
ENST00000485531.1:n.181A>C
ENST00000487381.5:n.214A>C
ENST00000489643.6:n.218A>C
ENST00000554085.5:c.188A>C ENSP00000450419.1:p.Lys63Thr
ENST00000554139.5:n.241A>C
ENST00000554330.5:n.185A>C
ENST00000554550.5:c.188A>C ENSP00000451435.1:p.Lys63Thr
ENST00000554638.5:n.212A>C
ENST00000554897.5:c.188A>C ENSP00000450942.1:p.Lys63Thr
ENST00000554944.5:n.218A>C
ENST00000555020.5:n.218A>C
ENST00000555086.5:n.192A>C
ENST00000555214.5:n.197A>C
ENST00000556157.1:n.295A>C
ENST00000556244.1:c.72A>C
ENST00000556278.1:c.188A>C ENSP00000451792.1:p.Lys63Thr
ENST00000556403.5:n.201A>C
ENST00000556494.5:n.220A>C
ENST00000557541.5:n.381A>C
ENST00000557706.5:n.302A>C
NM_000155.3:c.188A>C NP_000146.2:p.Lys63Thr
NM_001258332.1:c.-15A>C NP_001245261.1:n.-15A>C
NM_000155.4:c.188A>C MANE Select NP_000146.2:p.Lys63Thr
NM_001258332.2:c.-15A>C NP_001245261.1:n.-15A>C