Canonical Allele Identifier: CA373278940
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647254G>C , CM000671.2:g.34647254G>C GRCh38
NC_000009.11:g.34647251G>C , CM000671.1:g.34647251G>C GRCh37
NC_000009.10:g.34637251G>C NCBI36
NG_009029.1:g.5617G>C
NG_028966.1:g.70G>C
NG_009029.2:g.5666G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.248G>C ENSP00000509954.1:p.Gly83Ala
ENST00000378842.8:c.248G>C MANE Select ENSP00000368119.4:p.Gly83Ala
ENST00000378842.7:c.248G>C ENSP00000368119.3:p.Gly83Ala
ENST00000450095.6:c.46G>C ENSP00000401956.2:p.Glu16Gln
ENST00000465543.6:n.587G>C
ENST00000468099.2:n.288G>C
ENST00000472111.5:n.289G>C
ENST00000473506.6:c.248G>C ENSP00000432839.2:p.Gly83Ala
ENST00000473529.5:n.295G>C
ENST00000485531.1:n.241G>C
ENST00000487381.5:n.274G>C
ENST00000489643.6:n.278G>C
ENST00000554085.5:c.248G>C ENSP00000450419.1:p.Gly83Ala
ENST00000554139.5:n.301G>C
ENST00000554330.5:n.245G>C
ENST00000554550.5:c.248G>C ENSP00000451435.1:p.Gly83Ala
ENST00000554638.5:n.272G>C
ENST00000554897.5:c.248G>C ENSP00000450942.1:p.Gly83Ala
ENST00000554944.5:n.278G>C
ENST00000555020.5:n.278G>C
ENST00000555086.5:n.252G>C
ENST00000555214.5:n.257G>C
ENST00000556157.1:n.355G>C
ENST00000556244.1:c.132G>C
ENST00000556278.1:c.248G>C ENSP00000451792.1:p.Gly83Ala
ENST00000556403.5:n.261G>C
ENST00000556494.5:n.280G>C
ENST00000557541.5:n.441G>C
ENST00000557706.5:n.362G>C
NM_000155.3:c.248G>C NP_000146.2:p.Gly83Ala
NM_001258332.1:c.46G>C NP_001245261.1:p.Glu16Gln
NM_000155.4:c.248G>C MANE Select NP_000146.2:p.Gly83Ala
NM_001258332.2:c.46G>C NP_001245261.1:p.Glu16Gln