Canonical Allele Identifier: CA1845639808

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648846C= , CM000671.2:g.34648846C=	GRCh38
NC_000009.11:g.34648843C= , CM000671.1:g.34648843C=	GRCh37
NC_000009.10:g.34638843C=	NCBI36
NG_028966.1:g.1662C=
NG_009029.2:g.7258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*360C=	ENSP00000509954.1:n.*360C=
ENST00000378842.8:c.772C= MANE Select	ENSP00000368119.4:p.Arg258=
ENST00000378842.7:c.772C=	ENSP00000368119.3:p.Arg258=
ENST00000450095.6:c.445C=	ENSP00000401956.2:p.Arg149=
ENST00000473506.6:c.*360C=	ENSP00000432839.2:n.*360C=
ENST00000489643.6:n.852C=
ENST00000554085.5:c.*516C=	ENSP00000450419.1:n.*516C=
ENST00000554550.5:c.*392C=	ENSP00000451435.1:n.*392C=
ENST00000554638.5:n.1244C=
ENST00000555020.5:n.1233C=
ENST00000555086.5:n.776C=
ENST00000555754.1:n.117C=
ENST00000556244.1:c.759C=
ENST00000556278.1:c.432+390C=	ENSP00000451792.1:n.432+390C=
ENST00000557706.5:n.1334C=
NM_000155.3:c.772C=	NP_000146.2:p.Arg258=
NM_001258332.1:c.445C=	NP_001245261.1:p.Arg149=
NM_000155.4:c.772C= MANE Select	NP_000146.2:p.Arg258=
NM_001258332.2:c.445C=	NP_001245261.1:p.Arg149=