Canonical Allele Identifier: CA1845635340

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647118C= , CM000671.2:g.34647118C=	GRCh38
NC_000009.11:g.34647115C= , CM000671.1:g.34647115C=	GRCh37
NC_000009.10:g.34637115C=	NCBI36
NG_009029.1:g.5481C=
NG_009029.2:g.5530C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.112C=	ENSP00000509954.1:p.Gln38=
ENST00000378842.8:c.112C= MANE Select	ENSP00000368119.4:p.Gln38=
ENST00000378842.7:c.112C=	ENSP00000368119.3:p.Gln38=
ENST00000450095.6:c.-91C=	ENSP00000401956.2:n.-91C=
ENST00000465543.6:n.451C=
ENST00000468099.2:n.155-3C=
ENST00000472111.5:n.153C=
ENST00000473506.6:c.112C=	ENSP00000432839.2:p.Gln38=
ENST00000473529.5:n.159C=
ENST00000485531.1:n.105C=
ENST00000487381.5:n.138C=
ENST00000489643.6:n.142C=
ENST00000554085.5:c.112C=	ENSP00000450419.1:p.Gln38=
ENST00000554139.5:n.165C=
ENST00000554330.5:n.109C=
ENST00000554550.5:c.112C=	ENSP00000451435.1:p.Gln38=
ENST00000554638.5:n.136C=
ENST00000554897.5:c.112C=	ENSP00000450942.1:p.Gln38=
ENST00000554944.5:n.142C=
ENST00000555020.5:n.142C=
ENST00000555086.5:n.116C=
ENST00000555214.5:n.121C=
ENST00000556157.1:n.219C=
ENST00000556278.1:c.112C=	ENSP00000451792.1:p.Gln38=
ENST00000556403.5:n.125C=
ENST00000556494.5:n.144C=
ENST00000557541.5:n.305C=
ENST00000557706.5:n.226C=
ENST00000605275.1:n.650C=
NM_000155.3:c.112C=	NP_000146.2:p.Gln38=
NM_001258332.1:c.-91C=	NP_001245261.1:n.-91C=
NM_000155.4:c.112C= MANE Select	NP_000146.2:p.Gln38=
NM_001258332.2:c.-91C=	NP_001245261.1:n.-91C=