Canonical Allele Identifier: CA1845636291

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647538C= , CM000671.2:g.34647538C=	GRCh38
NC_000009.11:g.34647535C= , CM000671.1:g.34647535C=	GRCh37
NC_000009.10:g.34637535C=	NCBI36
NG_009029.1:g.5901C=
NG_028966.1:g.354C=
NG_009029.2:g.5950C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.299C=	ENSP00000509954.1:p.Pro100=
ENST00000378842.8:c.299C= MANE Select	ENSP00000368119.4:p.Pro100=
ENST00000378842.7:c.299C=	ENSP00000368119.3:p.Pro100=
ENST00000450095.6:c.50+280C=	ENSP00000401956.2:n.50+280C=
ENST00000465543.6:n.638C=
ENST00000472111.5:n.340C=
ENST00000473506.6:c.253-3C=	ENSP00000432839.2:n.253-3C=
ENST00000473529.5:n.346C=
ENST00000485531.1:n.525C=
ENST00000487381.5:n.558C=
ENST00000489643.6:n.282+280C=
ENST00000554085.5:c.*43C=	ENSP00000450419.1:n.*43C=
ENST00000554139.5:n.352C=
ENST00000554330.5:n.250-3C=
ENST00000554550.5:c.252+280C=	ENSP00000451435.1:n.252+280C=
ENST00000554638.5:n.556C=
ENST00000554897.5:c.252+280C=	ENSP00000450942.1:n.252+280C=
ENST00000554944.5:n.283-3C=
ENST00000555020.5:n.329C=
ENST00000555086.5:n.303C=
ENST00000555214.5:n.261+280C=
ENST00000556157.1:n.423C=
ENST00000556244.1:c.286C=
ENST00000556278.1:c.252+280C=	ENSP00000451792.1:n.252+280C=
ENST00000556403.5:n.312C=
ENST00000556494.5:n.331C=
ENST00000557541.5:n.446-3C=
ENST00000557706.5:n.646C=
NM_000155.3:c.299C=	NP_000146.2:p.Pro100=
NM_001258332.1:c.50+280C=	NP_001245261.1:n.50+280C=
NM_000155.4:c.299C= MANE Select	NP_000146.2:p.Pro100=
NM_001258332.2:c.50+280C=	NP_001245261.1:n.50+280C=