Canonical Allele Identifier: CA1845637774

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648043C= , CM000671.2:g.34648043C=	GRCh38
NC_000009.11:g.34648040C= , CM000671.1:g.34648040C=	GRCh37
NC_000009.10:g.34638040C=	NCBI36
NG_009029.1:g.6406C=
NG_028966.1:g.859C=
NG_009029.2:g.6455C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*96-72C=	ENSP00000509954.1:n.*96-72C=
ENST00000378842.8:c.508-72C= MANE Select	ENSP00000368119.4:n.508-72C=
ENST00000378842.7:c.508-72C=	ENSP00000368119.3:n.508-72C=
ENST00000450095.6:c.181-72C=	ENSP00000401956.2:n.181-72C=
ENST00000465543.6:n.847-72C=
ENST00000472111.5:n.764-72C=
ENST00000473506.6:c.*96-72C=	ENSP00000432839.2:n.*96-72C=
ENST00000473529.5:n.644-49C=
ENST00000485531.1:n.1030C=
ENST00000487381.5:n.893-72C=
ENST00000489643.6:n.283-72C=
ENST00000554085.5:c.*252-72C=	ENSP00000450419.1:n.*252-72C=
ENST00000554139.5:n.687-5C=
ENST00000554550.5:c.*128-72C=	ENSP00000451435.1:n.*128-72C=
ENST00000554638.5:n.980-72C=
ENST00000554897.5:c.*128-5C=	ENSP00000450942.1:n.*128-5C=
ENST00000554944.5:n.785C=
ENST00000555020.5:n.664-72C=
ENST00000555086.5:n.512-72C=
ENST00000555214.5:n.262-5C=
ENST00000556244.1:c.495-72C=
ENST00000556278.1:c.253-72C=	ENSP00000451792.1:n.253-72C=
ENST00000556494.5:n.629-72C=
ENST00000557706.5:n.1070-72C=
NM_000155.3:c.508-72C=	NP_000146.2:n.508-72C=
NM_001258332.1:c.181-72C=	NP_001245261.1:n.181-72C=
NM_000155.4:c.508-72C= MANE Select	NP_000146.2:n.508-72C=
NM_001258332.2:c.181-72C=	NP_001245261.1:n.181-72C=