Canonical Allele Identifier: CA1845635803
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647255A= , CM000671.2:g.34647255A= GRCh38
NC_000009.11:g.34647252A= , CM000671.1:g.34647252A= GRCh37
NC_000009.10:g.34637252A= NCBI36
NG_009029.1:g.5618A=
NG_028966.1:g.71A=
NG_009029.2:g.5667A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.249A= ENSP00000509954.1:p.Gly83=
ENST00000378842.8:c.249A= MANE Select ENSP00000368119.4:p.Gly83=
ENST00000378842.7:c.249A= ENSP00000368119.3:p.Gly83=
ENST00000450095.6:c.47A= ENSP00000401956.2:p.Glu16=
ENST00000465543.6:n.588A=
ENST00000468099.2:n.289A=
ENST00000472111.5:n.290A=
ENST00000473506.6:c.249A= ENSP00000432839.2:p.Gly83=
ENST00000473529.5:n.296A=
ENST00000485531.1:n.242A=
ENST00000487381.5:n.275A=
ENST00000489643.6:n.279A=
ENST00000554085.5:c.249A= ENSP00000450419.1:p.Gly83=
ENST00000554139.5:n.302A=
ENST00000554330.5:n.246A=
ENST00000554550.5:c.249A= ENSP00000451435.1:p.Gly83=
ENST00000554638.5:n.273A=
ENST00000554897.5:c.249A= ENSP00000450942.1:p.Gly83=
ENST00000554944.5:n.279A=
ENST00000555020.5:n.279A=
ENST00000555086.5:n.253A=
ENST00000555214.5:n.258A=
ENST00000556157.1:n.356A=
ENST00000556244.1:c.133A=
ENST00000556278.1:c.249A= ENSP00000451792.1:p.Gly83=
ENST00000556403.5:n.262A=
ENST00000556494.5:n.281A=
ENST00000557541.5:n.442A=
ENST00000557706.5:n.363A=
NM_000155.3:c.249A= NP_000146.2:p.Gly83=
NM_001258332.1:c.47A= NP_001245261.1:p.Glu16=
NM_000155.4:c.249A= MANE Select NP_000146.2:p.Gly83=
NM_001258332.2:c.47A= NP_001245261.1:p.Glu16=