Canonical Allele Identifier: CA1845638699

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648370C= , CM000671.2:g.34648370C=	GRCh38
NC_000009.11:g.34648367C= , CM000671.1:g.34648367C=	GRCh37
NC_000009.10:g.34638367C=	NCBI36
NG_009029.1:g.6733C=
NG_028966.1:g.1186C=
NG_009029.2:g.6782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*189C=	ENSP00000509954.1:n.*189C=
ENST00000378842.8:c.601C= MANE Select	ENSP00000368119.4:p.Arg201=
ENST00000378842.7:c.601C=	ENSP00000368119.3:p.Arg201=
ENST00000450095.6:c.274C=	ENSP00000401956.2:p.Arg92=
ENST00000472111.5:n.857C=
ENST00000473506.6:c.*189C=	ENSP00000432839.2:n.*189C=
ENST00000473529.5:n.760C=
ENST00000485531.1:n.1195C=
ENST00000487381.5:n.986C=
ENST00000489643.6:n.376C=
ENST00000554085.5:c.*345C=	ENSP00000450419.1:n.*345C=
ENST00000554139.5:n.847C=
ENST00000554550.5:c.*221C=	ENSP00000451435.1:n.*221C=
ENST00000554638.5:n.1073C=
ENST00000554897.5:c.*288C=	ENSP00000450942.1:n.*288C=
ENST00000554944.5:n.950C=
ENST00000555020.5:n.757C=
ENST00000555086.5:n.605C=
ENST00000555214.5:n.422C=
ENST00000556244.1:c.588C=
ENST00000556278.1:c.346C=	ENSP00000451792.1:p.Arg116=
ENST00000556494.5:n.722C=
ENST00000557706.5:n.1163C=
NM_000155.3:c.601C=	NP_000146.2:p.Arg201=
NM_001258332.1:c.274C=	NP_001245261.1:p.Arg92=
NM_000155.4:c.601C= MANE Select	NP_000146.2:p.Arg201=
NM_001258332.2:c.274C=	NP_001245261.1:p.Arg92=