Canonical Allele Identifier: CA652737211

Gene: GALT

Linked Data

• COSMIC: COSN18285078

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647781A>G , CM000671.2:g.34647781A>G	GRCh38
NC_000009.11:g.34647778A>G , CM000671.1:g.34647778A>G	GRCh37
NC_000009.10:g.34637778A>G	NCBI36
NG_009029.1:g.6144A>G
NG_028966.1:g.597A>G
NG_009029.2:g.6193A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-51A>G	ENSP00000509954.1:n.329-51A>G
ENST00000378842.8:c.378-51A>G MANE Select	ENSP00000368119.4:n.378-51A>G
ENST00000378842.7:c.378-51A>G	ENSP00000368119.3:n.378-51A>G
ENST00000450095.6:c.51-51A>G	ENSP00000401956.2:n.51-51A>G
ENST00000465543.6:n.717-51A>G
ENST00000472111.5:n.583A>G
ENST00000473506.6:c.329-51A>G	ENSP00000432839.2:n.329-51A>G
ENST00000473529.5:n.514-51A>G
ENST00000485531.1:n.768A>G
ENST00000487381.5:n.712A>G
ENST00000489643.6:n.283-334A>G
ENST00000554085.5:c.*122-51A>G	ENSP00000450419.1:n.*122-51A>G
ENST00000554139.5:n.506A>G
ENST00000554330.5:n.490A>G
ENST00000554550.5:c.253-51A>G	ENSP00000451435.1:n.253-51A>G
ENST00000554638.5:n.799A>G
ENST00000554897.5:c.253-51A>G	ENSP00000450942.1:n.253-51A>G
ENST00000554944.5:n.523A>G
ENST00000555020.5:n.483A>G
ENST00000555086.5:n.382-51A>G
ENST00000555214.5:n.262-267A>G
ENST00000556244.1:c.365-51A>G
ENST00000556278.1:c.253-334A>G	ENSP00000451792.1:n.253-334A>G
ENST00000556403.5:n.555A>G
ENST00000556494.5:n.499-51A>G
ENST00000557541.5:n.522-51A>G
ENST00000557706.5:n.889A>G
NM_000155.3:c.378-51A>G	NP_000146.2:n.378-51A>G
NM_001258332.1:c.51-51A>G	NP_001245261.1:n.51-51A>G
NM_000155.4:c.378-51A>G MANE Select	NP_000146.2:n.378-51A>G
NM_001258332.2:c.51-51A>G	NP_001245261.1:n.51-51A>G