Canonical Allele Identifier: CA2689808684
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34648054-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648054G>A , CM000671.2:g.34648054G>A GRCh38
NC_000009.11:g.34648051G>A , CM000671.1:g.34648051G>A GRCh37
NC_000009.10:g.34638051G>A NCBI36
NG_009029.1:g.6417G>A
NG_028966.1:g.870G>A
NG_009029.2:g.6466G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*96-61G>A ENSP00000509954.1:n.*96-61G>A
ENST00000378842.8:c.508-61G>A MANE Select ENSP00000368119.4:n.508-61G>A
ENST00000378842.7:c.508-61G>A ENSP00000368119.3:n.508-61G>A
ENST00000450095.6:c.181-61G>A ENSP00000401956.2:n.181-61G>A
ENST00000465543.6:n.847-61G>A
ENST00000472111.5:n.764-61G>A
ENST00000473506.6:c.*96-61G>A ENSP00000432839.2:n.*96-61G>A
ENST00000473529.5:n.644-38G>A
ENST00000485531.1:n.1041G>A
ENST00000487381.5:n.893-61G>A
ENST00000489643.6:n.283-61G>A
ENST00000554085.5:c.*252-61G>A ENSP00000450419.1:n.*252-61G>A
ENST00000554139.5:n.693G>A
ENST00000554550.5:c.*128-61G>A ENSP00000451435.1:n.*128-61G>A
ENST00000554638.5:n.980-61G>A
ENST00000554897.5:c.*134G>A ENSP00000450942.1:n.*134G>A
ENST00000554944.5:n.796G>A
ENST00000555020.5:n.664-61G>A
ENST00000555086.5:n.512-61G>A
ENST00000555214.5:n.268G>A
ENST00000556244.1:c.495-61G>A
ENST00000556278.1:c.253-61G>A ENSP00000451792.1:n.253-61G>A
ENST00000556494.5:n.629-61G>A
ENST00000557706.5:n.1070-61G>A
NM_000155.3:c.508-61G>A NP_000146.2:n.508-61G>A
NM_001258332.1:c.181-61G>A NP_001245261.1:n.181-61G>A
NM_000155.4:c.508-61G>A MANE Select NP_000146.2:n.508-61G>A
NM_001258332.2:c.181-61G>A NP_001245261.1:n.181-61G>A