Canonical Allele Identifier: CA1845639901

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648862G= , CM000671.2:g.34648862G=	GRCh38
NC_000009.11:g.34648859G= , CM000671.1:g.34648859G=	GRCh37
NC_000009.10:g.34638859G=	NCBI36
NG_009029.1:g.7225G=
NG_028966.1:g.1678G=
NG_009029.2:g.7274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*376G=	ENSP00000509954.1:n.*376G=
ENST00000378842.8:c.788G= MANE Select	ENSP00000368119.4:p.Arg263=
ENST00000378842.7:c.788G=	ENSP00000368119.3:p.Arg263=
ENST00000450095.6:c.461G=	ENSP00000401956.2:p.Arg154=
ENST00000473506.6:c.*376G=	ENSP00000432839.2:n.*376G=
ENST00000489643.6:n.868G=
ENST00000554085.5:c.*532G=	ENSP00000450419.1:n.*532G=
ENST00000554550.5:c.*408G=	ENSP00000451435.1:n.*408G=
ENST00000554638.5:n.1260G=
ENST00000555020.5:n.1249G=
ENST00000555086.5:n.792G=
ENST00000555754.1:n.133G=
ENST00000556244.1:c.775G=
ENST00000556278.1:c.432+406G=	ENSP00000451792.1:n.432+406G=
ENST00000557706.5:n.1350G=
NM_000155.3:c.788G=	NP_000146.2:p.Arg263=
NM_001258332.1:c.461G=	NP_001245261.1:p.Arg154=
NM_000155.4:c.788G= MANE Select	NP_000146.2:p.Arg263=
NM_001258332.2:c.461G=	NP_001245261.1:p.Arg154=