Canonical Allele Identifier: CA1845639082

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648452G= , CM000671.2:g.34648452G=	GRCh38
NC_000009.11:g.34648449G= , CM000671.1:g.34648449G=	GRCh37
NC_000009.10:g.34638449G=	NCBI36
NG_009029.1:g.6815G=
NG_028966.1:g.1268G=
NG_009029.2:g.6864G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*271G=	ENSP00000509954.1:n.*271G=
ENST00000378842.8:c.683G= MANE Select	ENSP00000368119.4:p.Arg228=
ENST00000378842.7:c.683G=	ENSP00000368119.3:p.Arg228=
ENST00000450095.6:c.356G=	ENSP00000401956.2:p.Arg119=
ENST00000472111.5:n.939G=
ENST00000473506.6:c.*271G=	ENSP00000432839.2:n.*271G=
ENST00000473529.5:n.842G=
ENST00000487381.5:n.1068G=
ENST00000489643.6:n.458G=
ENST00000554085.5:c.*427G=	ENSP00000450419.1:n.*427G=
ENST00000554550.5:c.*303G=	ENSP00000451435.1:n.*303G=
ENST00000554638.5:n.1155G=
ENST00000555020.5:n.839G=
ENST00000555086.5:n.687G=
ENST00000555214.5:n.504G=
ENST00000555754.1:n.28G=
ENST00000556244.1:c.670G=
ENST00000556278.1:c.428G=	ENSP00000451792.1:p.Arg143=
ENST00000556494.5:n.804G=
ENST00000557706.5:n.1245G=
NM_000155.3:c.683G=	NP_000146.2:p.Arg228=
NM_001258332.1:c.356G=	NP_001245261.1:p.Arg119=
NM_000155.4:c.683G= MANE Select	NP_000146.2:p.Arg228=
NM_001258332.2:c.356G=	NP_001245261.1:p.Arg119=