Canonical Allele Identifier: CA1845637806

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648066T= , CM000671.2:g.34648066T=	GRCh38
NC_000009.11:g.34648063T= , CM000671.1:g.34648063T=	GRCh37
NC_000009.10:g.34638063T=	NCBI36
NG_009029.1:g.6429T=
NG_028966.1:g.882T=
NG_009029.2:g.6478T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*96-49T=	ENSP00000509954.1:n.*96-49T=
ENST00000378842.8:c.508-49T= MANE Select	ENSP00000368119.4:n.508-49T=
ENST00000378842.7:c.508-49T=	ENSP00000368119.3:n.508-49T=
ENST00000450095.6:c.181-49T=	ENSP00000401956.2:n.181-49T=
ENST00000465543.6:n.847-49T=
ENST00000472111.5:n.764-49T=
ENST00000473506.6:c.*96-49T=	ENSP00000432839.2:n.*96-49T=
ENST00000473529.5:n.644-26T=
ENST00000485531.1:n.1053T=
ENST00000487381.5:n.893-49T=
ENST00000489643.6:n.283-49T=
ENST00000554085.5:c.*252-49T=	ENSP00000450419.1:n.*252-49T=
ENST00000554139.5:n.705T=
ENST00000554550.5:c.*128-49T=	ENSP00000451435.1:n.*128-49T=
ENST00000554638.5:n.980-49T=
ENST00000554897.5:c.*146T=	ENSP00000450942.1:n.*146T=
ENST00000554944.5:n.808T=
ENST00000555020.5:n.664-49T=
ENST00000555086.5:n.512-49T=
ENST00000555214.5:n.280T=
ENST00000556244.1:c.495-49T=
ENST00000556278.1:c.253-49T=	ENSP00000451792.1:n.253-49T=
ENST00000556494.5:n.629-49T=
ENST00000557706.5:n.1070-49T=
NM_000155.3:c.508-49T=	NP_000146.2:n.508-49T=
NM_001258332.1:c.181-49T=	NP_001245261.1:n.181-49T=
NM_000155.4:c.508-49T= MANE Select	NP_000146.2:n.508-49T=
NM_001258332.2:c.181-49T=	NP_001245261.1:n.181-49T=