Canonical Allele Identifier: CA1845636373
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821138104

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647595A>G , CM000671.2:g.34647595A>G GRCh38
NC_000009.11:g.34647592A>G , CM000671.1:g.34647592A>G GRCh37
NC_000009.10:g.34637592A>G NCBI36
NG_009029.1:g.5958A>G
NG_028966.1:g.411A>G
NG_009029.2:g.6007A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.328+28A>G ENSP00000509954.1:n.328+28A>G
ENST00000378842.8:c.328+28A>G MANE Select ENSP00000368119.4:n.328+28A>G
ENST00000378842.7:c.328+28A>G ENSP00000368119.3:n.328+28A>G
ENST00000450095.6:c.51-237A>G ENSP00000401956.2:n.51-237A>G
ENST00000465543.6:n.667+28A>G
ENST00000472111.5:n.397A>G
ENST00000473506.6:c.279+28A>G ENSP00000432839.2:n.279+28A>G
ENST00000473529.5:n.403A>G
ENST00000485531.1:n.582A>G
ENST00000487381.5:n.587+28A>G
ENST00000489643.6:n.282+337A>G
ENST00000554085.5:c.*72+28A>G ENSP00000450419.1:n.*72+28A>G
ENST00000554139.5:n.381+28A>G
ENST00000554330.5:n.304A>G
ENST00000554550.5:c.253-237A>G ENSP00000451435.1:n.253-237A>G
ENST00000554638.5:n.613A>G
ENST00000554897.5:c.253-237A>G ENSP00000450942.1:n.253-237A>G
ENST00000554944.5:n.337A>G
ENST00000555020.5:n.358+28A>G
ENST00000555086.5:n.332+28A>G
ENST00000555214.5:n.261+337A>G
ENST00000556157.1:n.452+28A>G
ENST00000556244.1:c.315+28A>G
ENST00000556278.1:c.252+337A>G ENSP00000451792.1:n.252+337A>G
ENST00000556403.5:n.369A>G
ENST00000556494.5:n.388A>G
ENST00000557541.5:n.472+28A>G
ENST00000557706.5:n.703A>G
NM_000155.3:c.328+28A>G NP_000146.2:n.328+28A>G
NM_001258332.1:c.51-237A>G NP_001245261.1:n.51-237A>G
NM_000155.4:c.328+28A>G MANE Select NP_000146.2:n.328+28A>G
NM_001258332.2:c.51-237A>G NP_001245261.1:n.51-237A>G