Canonical Allele Identifier: CA1845638971

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648427G= , CM000671.2:g.34648427G=	GRCh38
NC_000009.11:g.34648424G= , CM000671.1:g.34648424G=	GRCh37
NC_000009.10:g.34638424G=	NCBI36
NG_009029.1:g.6790G=
NG_028966.1:g.1243G=
NG_009029.2:g.6839G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*246G=	ENSP00000509954.1:n.*246G=
ENST00000378842.8:c.658G= MANE Select	ENSP00000368119.4:p.Glu220=
ENST00000378842.7:c.658G=	ENSP00000368119.3:p.Glu220=
ENST00000450095.6:c.331G=	ENSP00000401956.2:p.Glu111=
ENST00000472111.5:n.914G=
ENST00000473506.6:c.*246G=	ENSP00000432839.2:n.*246G=
ENST00000473529.5:n.817G=
ENST00000487381.5:n.1043G=
ENST00000489643.6:n.433G=
ENST00000554085.5:c.*402G=	ENSP00000450419.1:n.*402G=
ENST00000554550.5:c.*278G=	ENSP00000451435.1:n.*278G=
ENST00000554638.5:n.1130G=
ENST00000555020.5:n.814G=
ENST00000555086.5:n.662G=
ENST00000555214.5:n.479G=
ENST00000555754.1:n.3G=
ENST00000556244.1:c.645G=
ENST00000556278.1:c.403G=	ENSP00000451792.1:p.Glu135=
ENST00000556494.5:n.779G=
ENST00000557706.5:n.1220G=
NM_000155.3:c.658G=	NP_000146.2:p.Glu220=
NM_001258332.1:c.331G=	NP_001245261.1:p.Glu111=
NM_000155.4:c.658G= MANE Select	NP_000146.2:p.Glu220=
NM_001258332.2:c.331G=	NP_001245261.1:p.Glu111=