Canonical Allele Identifier: CA1845638732

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648379C= , CM000671.2:g.34648379C=	GRCh38
NC_000009.11:g.34648376C= , CM000671.1:g.34648376C=	GRCh37
NC_000009.10:g.34638376C=	NCBI36
NG_009029.1:g.6742C=
NG_028966.1:g.1195C=
NG_009029.2:g.6791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*198C=	ENSP00000509954.1:n.*198C=
ENST00000378842.8:c.610C= MANE Select	ENSP00000368119.4:p.Arg204=
ENST00000378842.7:c.610C=	ENSP00000368119.3:p.Arg204=
ENST00000450095.6:c.283C=	ENSP00000401956.2:p.Arg95=
ENST00000472111.5:n.866C=
ENST00000473506.6:c.*198C=	ENSP00000432839.2:n.*198C=
ENST00000473529.5:n.769C=
ENST00000487381.5:n.995C=
ENST00000489643.6:n.385C=
ENST00000554085.5:c.*354C=	ENSP00000450419.1:n.*354C=
ENST00000554139.5:n.856C=
ENST00000554550.5:c.*230C=	ENSP00000451435.1:n.*230C=
ENST00000554638.5:n.1082C=
ENST00000554944.5:n.959C=
ENST00000555020.5:n.766C=
ENST00000555086.5:n.614C=
ENST00000555214.5:n.431C=
ENST00000556244.1:c.597C=
ENST00000556278.1:c.355C=	ENSP00000451792.1:p.Arg119=
ENST00000556494.5:n.731C=
ENST00000557706.5:n.1172C=
NM_000155.3:c.610C=	NP_000146.2:p.Arg204=
NM_001258332.1:c.283C=	NP_001245261.1:p.Arg95=
NM_000155.4:c.610C= MANE Select	NP_000146.2:p.Arg204=
NM_001258332.2:c.283C=	NP_001245261.1:p.Arg95=