Canonical Allele Identifier: CA1845637384

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647911G= , CM000671.2:g.34647911G=	GRCh38
NC_000009.11:g.34647908G= , CM000671.1:g.34647908G=	GRCh37
NC_000009.10:g.34637908G=	NCBI36
NG_009029.1:g.6274G=
NG_028966.1:g.727G=
NG_009029.2:g.6323G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*45G=	ENSP00000509954.1:n.*45G=
ENST00000378842.8:c.457G= MANE Select	ENSP00000368119.4:p.Ala153=
ENST00000378842.7:c.457G=	ENSP00000368119.3:p.Ala153=
ENST00000450095.6:c.130G=	ENSP00000401956.2:p.Ala44=
ENST00000465543.6:n.796G=
ENST00000472111.5:n.713G=
ENST00000473506.6:c.*45G=	ENSP00000432839.2:n.*45G=
ENST00000473529.5:n.593G=
ENST00000485531.1:n.898G=
ENST00000487381.5:n.842G=
ENST00000489643.6:n.283-204G=
ENST00000554085.5:c.*201G=	ENSP00000450419.1:n.*201G=
ENST00000554139.5:n.636G=
ENST00000554550.5:c.*77G=	ENSP00000451435.1:n.*77G=
ENST00000554638.5:n.929G=
ENST00000554897.5:c.*77G=	ENSP00000450942.1:n.*77G=
ENST00000554944.5:n.653G=
ENST00000555020.5:n.613G=
ENST00000555086.5:n.461G=
ENST00000555214.5:n.262-137G=
ENST00000556244.1:c.444G=
ENST00000556278.1:c.253-204G=	ENSP00000451792.1:n.253-204G=
ENST00000556494.5:n.578G=
ENST00000557706.5:n.1019G=
NM_000155.3:c.457G=	NP_000146.2:p.Ala153=
NM_001258332.1:c.130G=	NP_001245261.1:p.Ala44=
NM_000155.4:c.457G= MANE Select	NP_000146.2:p.Ala153=
NM_001258332.2:c.130G=	NP_001245261.1:p.Ala44=