Canonical Allele Identifier: CA2509895047

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647654C>A , CM000671.2:g.34647654C>A	GRCh38
NC_000009.11:g.34647651C>A , CM000671.1:g.34647651C>A	GRCh37
NC_000009.10:g.34637651C>A	NCBI36
NG_009029.1:g.6017C>A
NG_028966.1:g.470C>A
NG_009029.2:g.6066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+87C>A	ENSP00000509954.1:n.328+87C>A
ENST00000378842.8:c.329-3C>A MANE Select	ENSP00000368119.4:n.329-3C>A
ENST00000378842.7:c.329-3C>A	ENSP00000368119.3:n.329-3C>A
ENST00000450095.6:c.51-178C>A	ENSP00000401956.2:n.51-178C>A
ENST00000465543.6:n.668-3C>A
ENST00000472111.5:n.456C>A
ENST00000473506.6:c.280-3C>A	ENSP00000432839.2:n.280-3C>A
ENST00000473529.5:n.462C>A
ENST00000485531.1:n.641C>A
ENST00000487381.5:n.588-3C>A
ENST00000489643.6:n.282+396C>A
ENST00000554085.5:c.*73-3C>A	ENSP00000450419.1:n.*73-3C>A
ENST00000554139.5:n.382-3C>A
ENST00000554330.5:n.363C>A
ENST00000554550.5:c.253-178C>A	ENSP00000451435.1:n.253-178C>A
ENST00000554638.5:n.672C>A
ENST00000554897.5:c.253-178C>A	ENSP00000450942.1:n.253-178C>A
ENST00000554944.5:n.396C>A
ENST00000555020.5:n.359-3C>A
ENST00000555086.5:n.333-3C>A
ENST00000555214.5:n.262-394C>A
ENST00000556157.1:n.453-3C>A
ENST00000556244.1:c.316-3C>A
ENST00000556278.1:c.252+396C>A	ENSP00000451792.1:n.252+396C>A
ENST00000556403.5:n.428C>A
ENST00000556494.5:n.447C>A
ENST00000557541.5:n.473-3C>A
ENST00000557706.5:n.762C>A
NM_000155.3:c.329-3C>A	NP_000146.2:n.329-3C>A
NM_001258332.1:c.51-178C>A	NP_001245261.1:n.51-178C>A
NM_000155.4:c.329-3C>A MANE Select	NP_000146.2:n.329-3C>A
NM_001258332.2:c.51-178C>A	NP_001245261.1:n.51-178C>A