Canonical Allele Identifier: CA2579371292

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648218C>A , CM000671.2:g.34648218C>A	GRCh38
NC_000009.11:g.34648215C>A , CM000671.1:g.34648215C>A	GRCh37
NC_000009.10:g.34638215C>A	NCBI36
NG_009029.1:g.6581C>A
NG_028966.1:g.1034C>A
NG_009029.2:g.6630C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*152+47C>A	ENSP00000509954.1:n.*152+47C>A
ENST00000378842.8:c.564+47C>A MANE Select	ENSP00000368119.4:n.564+47C>A
ENST00000378842.7:c.564+47C>A	ENSP00000368119.3:n.564+47C>A
ENST00000450095.6:c.237+47C>A	ENSP00000401956.2:n.237+47C>A
ENST00000472111.5:n.820+47C>A
ENST00000473506.6:c.*152+47C>A	ENSP00000432839.2:n.*152+47C>A
ENST00000473529.5:n.723+47C>A
ENST00000485531.1:n.1158+47C>A
ENST00000487381.5:n.949+47C>A
ENST00000489643.6:n.339+47C>A
ENST00000554085.5:c.*308+47C>A	ENSP00000450419.1:n.*308+47C>A
ENST00000554139.5:n.810+47C>A
ENST00000554550.5:c.*184+47C>A	ENSP00000451435.1:n.*184+47C>A
ENST00000554638.5:n.1036+47C>A
ENST00000554897.5:c.*251+47C>A	ENSP00000450942.1:n.*251+47C>A
ENST00000554944.5:n.913+47C>A
ENST00000555020.5:n.720+47C>A
ENST00000555086.5:n.568+47C>A
ENST00000555214.5:n.385+47C>A
ENST00000556244.1:c.551+47C>A
ENST00000556278.1:c.309+47C>A	ENSP00000451792.1:n.309+47C>A
ENST00000556494.5:n.685+47C>A
ENST00000557706.5:n.1126+47C>A
NM_000155.3:c.564+47C>A	NP_000146.2:n.564+47C>A
NM_001258332.1:c.237+47C>A	NP_001245261.1:n.237+47C>A
NM_000155.4:c.564+47C>A MANE Select	NP_000146.2:n.564+47C>A
NM_001258332.2:c.237+47C>A	NP_001245261.1:n.237+47C>A