Canonical Allele Identifier: CA1845638590
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648349T= , CM000671.2:g.34648349T= GRCh38
NC_000009.11:g.34648346T= , CM000671.1:g.34648346T= GRCh37
NC_000009.10:g.34638346T= NCBI36
NG_009029.1:g.6712T=
NG_028966.1:g.1165T=
NG_009029.2:g.6761T=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*168T= ENSP00000509954.1:n.*168T=
ENST00000378842.8:c.580T= MANE Select ENSP00000368119.4:p.Phe194=
ENST00000378842.7:c.580T= ENSP00000368119.3:p.Phe194=
ENST00000450095.6:c.253T= ENSP00000401956.2:p.Phe85=
ENST00000472111.5:n.836T=
ENST00000473506.6:c.*168T= ENSP00000432839.2:n.*168T=
ENST00000473529.5:n.739T=
ENST00000485531.1:n.1174T=
ENST00000487381.5:n.965T=
ENST00000489643.6:n.355T=
ENST00000554085.5:c.*324T= ENSP00000450419.1:n.*324T=
ENST00000554139.5:n.826T=
ENST00000554550.5:c.*200T= ENSP00000451435.1:n.*200T=
ENST00000554638.5:n.1052T=
ENST00000554897.5:c.*267T= ENSP00000450942.1:n.*267T=
ENST00000554944.5:n.929T=
ENST00000555020.5:n.736T=
ENST00000555086.5:n.584T=
ENST00000555214.5:n.401T=
ENST00000556244.1:c.567T=
ENST00000556278.1:c.325T= ENSP00000451792.1:p.Phe109=
ENST00000556494.5:n.701T=
ENST00000557706.5:n.1142T=
NM_000155.3:c.580T= NP_000146.2:p.Phe194=
NM_001258332.1:c.253T= NP_001245261.1:p.Phe85=
NM_000155.4:c.580T= MANE Select NP_000146.2:p.Phe194=
NM_001258332.2:c.253T= NP_001245261.1:p.Phe85=