Canonical Allele Identifier: CA1845635780

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647243C= , CM000671.2:g.34647243C=	GRCh38
NC_000009.11:g.34647240C= , CM000671.1:g.34647240C=	GRCh37
NC_000009.10:g.34637240C=	NCBI36
NG_009029.1:g.5606C=
NG_028966.1:g.59C=
NG_009029.2:g.5655C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.237C=	ENSP00000509954.1:p.Ile79=
ENST00000378842.8:c.237C= MANE Select	ENSP00000368119.4:p.Ile79=
ENST00000378842.7:c.237C=	ENSP00000368119.3:p.Ile79=
ENST00000450095.6:c.35C=	ENSP00000401956.2:p.Ser12=
ENST00000465543.6:n.576C=
ENST00000468099.2:n.277C=
ENST00000472111.5:n.278C=
ENST00000473506.6:c.237C=	ENSP00000432839.2:p.Ile79=
ENST00000473529.5:n.284C=
ENST00000485531.1:n.230C=
ENST00000487381.5:n.263C=
ENST00000489643.6:n.267C=
ENST00000554085.5:c.237C=	ENSP00000450419.1:p.Ile79=
ENST00000554139.5:n.290C=
ENST00000554330.5:n.234C=
ENST00000554550.5:c.237C=	ENSP00000451435.1:p.Ile79=
ENST00000554638.5:n.261C=
ENST00000554897.5:c.237C=	ENSP00000450942.1:p.Ile79=
ENST00000554944.5:n.267C=
ENST00000555020.5:n.267C=
ENST00000555086.5:n.241C=
ENST00000555214.5:n.246C=
ENST00000556157.1:n.344C=
ENST00000556244.1:c.121C=
ENST00000556278.1:c.237C=	ENSP00000451792.1:p.Ile79=
ENST00000556403.5:n.250C=
ENST00000556494.5:n.269C=
ENST00000557541.5:n.430C=
ENST00000557706.5:n.351C=
NM_000155.3:c.237C=	NP_000146.2:p.Ile79=
NM_001258332.1:c.35C=	NP_001245261.1:p.Ser12=
NM_000155.4:c.237C= MANE Select	NP_000146.2:p.Ile79=
NM_001258332.2:c.35C=	NP_001245261.1:p.Ser12=