Canonical Allele Identifier: CA373278684
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647185A>G , CM000671.2:g.34647185A>G GRCh38
NC_000009.11:g.34647182A>G , CM000671.1:g.34647182A>G GRCh37
NC_000009.10:g.34637182A>G NCBI36
NG_009029.1:g.5548A>G
NG_028966.1:g.1A>G
NG_009029.2:g.5597A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.179A>G ENSP00000509954.1:p.Gln60Arg
ENST00000378842.8:c.179A>G MANE Select ENSP00000368119.4:p.Gln60Arg
ENST00000378842.7:c.179A>G ENSP00000368119.3:p.Gln60Arg
ENST00000450095.6:c.-24A>G ENSP00000401956.2:n.-24A>G
ENST00000465543.6:n.518A>G
ENST00000468099.2:n.219A>G
ENST00000472111.5:n.220A>G
ENST00000473506.6:c.179A>G ENSP00000432839.2:p.Gln60Arg
ENST00000473529.5:n.226A>G
ENST00000485531.1:n.172A>G
ENST00000487381.5:n.205A>G
ENST00000489643.6:n.209A>G
ENST00000554085.5:c.179A>G ENSP00000450419.1:p.Gln60Arg
ENST00000554139.5:n.232A>G
ENST00000554330.5:n.176A>G
ENST00000554550.5:c.179A>G ENSP00000451435.1:p.Gln60Arg
ENST00000554638.5:n.203A>G
ENST00000554897.5:c.179A>G ENSP00000450942.1:p.Gln60Arg
ENST00000554944.5:n.209A>G
ENST00000555020.5:n.209A>G
ENST00000555086.5:n.183A>G
ENST00000555214.5:n.188A>G
ENST00000556157.1:n.286A>G
ENST00000556244.1:c.63A>G
ENST00000556278.1:c.179A>G ENSP00000451792.1:p.Gln60Arg
ENST00000556403.5:n.192A>G
ENST00000556494.5:n.211A>G
ENST00000557541.5:n.372A>G
ENST00000557706.5:n.293A>G
NM_000155.3:c.179A>G NP_000146.2:p.Gln60Arg
NM_001258332.1:c.-24A>G NP_001245261.1:n.-24A>G
NM_000155.4:c.179A>G MANE Select NP_000146.2:p.Gln60Arg
NM_001258332.2:c.-24A>G NP_001245261.1:n.-24A>G