Canonical Allele Identifier: CA1845639853

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648851G= , CM000671.2:g.34648851G=	GRCh38
NC_000009.11:g.34648848G= , CM000671.1:g.34648848G=	GRCh37
NC_000009.10:g.34638848G=	NCBI36
NG_028966.1:g.1667G=
NG_009029.2:g.7263G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*365G=	ENSP00000509954.1:n.*365G=
ENST00000378842.8:c.777G= MANE Select	ENSP00000368119.4:p.Arg259=
ENST00000378842.7:c.777G=	ENSP00000368119.3:p.Arg259=
ENST00000450095.6:c.450G=	ENSP00000401956.2:p.Arg150=
ENST00000473506.6:c.*365G=	ENSP00000432839.2:n.*365G=
ENST00000489643.6:n.857G=
ENST00000554085.5:c.*521G=	ENSP00000450419.1:n.*521G=
ENST00000554550.5:c.*397G=	ENSP00000451435.1:n.*397G=
ENST00000554638.5:n.1249G=
ENST00000555020.5:n.1238G=
ENST00000555086.5:n.781G=
ENST00000555754.1:n.122G=
ENST00000556244.1:c.764G=
ENST00000556278.1:c.432+395G=	ENSP00000451792.1:n.432+395G=
ENST00000557706.5:n.1339G=
NM_000155.3:c.777G=	NP_000146.2:p.Arg259=
NM_001258332.1:c.450G=	NP_001245261.1:p.Arg150=
NM_000155.4:c.777G= MANE Select	NP_000146.2:p.Arg259=
NM_001258332.2:c.450G=	NP_001245261.1:p.Arg150=