Canonical Allele Identifier: CA1845635783

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647244C= , CM000671.2:g.34647244C=	GRCh38
NC_000009.11:g.34647241C= , CM000671.1:g.34647241C=	GRCh37
NC_000009.10:g.34637241C=	NCBI36
NG_009029.1:g.5607C=
NG_028966.1:g.60C=
NG_009029.2:g.5656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.238C=	ENSP00000509954.1:p.Arg80=
ENST00000378842.8:c.238C= MANE Select	ENSP00000368119.4:p.Arg80=
ENST00000378842.7:c.238C=	ENSP00000368119.3:p.Arg80=
ENST00000450095.6:c.36C=	ENSP00000401956.2:p.Ser12=
ENST00000465543.6:n.577C=
ENST00000468099.2:n.278C=
ENST00000472111.5:n.279C=
ENST00000473506.6:c.238C=	ENSP00000432839.2:p.Arg80=
ENST00000473529.5:n.285C=
ENST00000485531.1:n.231C=
ENST00000487381.5:n.264C=
ENST00000489643.6:n.268C=
ENST00000554085.5:c.238C=	ENSP00000450419.1:p.Arg80=
ENST00000554139.5:n.291C=
ENST00000554330.5:n.235C=
ENST00000554550.5:c.238C=	ENSP00000451435.1:p.Arg80=
ENST00000554638.5:n.262C=
ENST00000554897.5:c.238C=	ENSP00000450942.1:p.Arg80=
ENST00000554944.5:n.268C=
ENST00000555020.5:n.268C=
ENST00000555086.5:n.242C=
ENST00000555214.5:n.247C=
ENST00000556157.1:n.345C=
ENST00000556244.1:c.122C=
ENST00000556278.1:c.238C=	ENSP00000451792.1:p.Arg80=
ENST00000556403.5:n.251C=
ENST00000556494.5:n.270C=
ENST00000557541.5:n.431C=
ENST00000557706.5:n.352C=
NM_000155.3:c.238C=	NP_000146.2:p.Arg80=
NM_001258332.1:c.36C=	NP_001245261.1:p.Ser12=
NM_000155.4:c.238C= MANE Select	NP_000146.2:p.Arg80=
NM_001258332.2:c.36C=	NP_001245261.1:p.Ser12=