Canonical Allele Identifier: CA1845638023

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648135C= , CM000671.2:g.34648135C=	GRCh38
NC_000009.11:g.34648132C= , CM000671.1:g.34648132C=	GRCh37
NC_000009.10:g.34638132C=	NCBI36
NG_009029.1:g.6498C=
NG_028966.1:g.951C=
NG_009029.2:g.6547C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*116C=	ENSP00000509954.1:n.*116C=
ENST00000378842.8:c.528C= MANE Select	ENSP00000368119.4:p.Ala176=
ENST00000378842.7:c.528C=	ENSP00000368119.3:p.Ala176=
ENST00000450095.6:c.201C=	ENSP00000401956.2:p.Ala67=
ENST00000465543.6:n.867C=
ENST00000472111.5:n.784C=
ENST00000473506.6:c.*116C=	ENSP00000432839.2:n.*116C=
ENST00000473529.5:n.687C=
ENST00000485531.1:n.1122C=
ENST00000487381.5:n.913C=
ENST00000489643.6:n.303C=
ENST00000554085.5:c.*272C=	ENSP00000450419.1:n.*272C=
ENST00000554139.5:n.774C=
ENST00000554550.5:c.*148C=	ENSP00000451435.1:n.*148C=
ENST00000554638.5:n.1000C=
ENST00000554897.5:c.*215C=	ENSP00000450942.1:n.*215C=
ENST00000554944.5:n.877C=
ENST00000555020.5:n.684C=
ENST00000555086.5:n.532C=
ENST00000555214.5:n.349C=
ENST00000556244.1:c.515C=
ENST00000556278.1:c.273C=	ENSP00000451792.1:p.Ala91=
ENST00000556494.5:n.649C=
ENST00000557706.5:n.1090C=
NM_000155.3:c.528C=	NP_000146.2:p.Ala176=
NM_001258332.1:c.201C=	NP_001245261.1:p.Ala67=
NM_000155.4:c.528C= MANE Select	NP_000146.2:p.Ala176=
NM_001258332.2:c.201C=	NP_001245261.1:p.Ala67=