Canonical Allele Identifier: CA1845639956

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648870G= , CM000671.2:g.34648870G=	GRCh38
NC_000009.11:g.34648867G= , CM000671.1:g.34648867G=	GRCh37
NC_000009.10:g.34638867G=	NCBI36
NG_009029.1:g.7233G=
NG_028966.1:g.1686G=
NG_009029.2:g.7282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*384G=	ENSP00000509954.1:n.*384G=
ENST00000378842.8:c.796G= MANE Select	ENSP00000368119.4:p.Glu266=
ENST00000378842.7:c.796G=	ENSP00000368119.3:p.Glu266=
ENST00000450095.6:c.469G=	ENSP00000401956.2:p.Glu157=
ENST00000473506.6:c.*384G=	ENSP00000432839.2:n.*384G=
ENST00000489643.6:n.876G=
ENST00000554085.5:c.*540G=	ENSP00000450419.1:n.*540G=
ENST00000554550.5:c.*416G=	ENSP00000451435.1:n.*416G=
ENST00000554638.5:n.1268G=
ENST00000555020.5:n.1257G=
ENST00000555086.5:n.800G=
ENST00000555754.1:n.141G=
ENST00000556244.1:c.783G=
ENST00000556278.1:c.432+414G=	ENSP00000451792.1:n.432+414G=
ENST00000557706.5:n.1358G=
NM_000155.3:c.796G=	NP_000146.2:p.Glu266=
NM_001258332.1:c.469G=	NP_001245261.1:p.Glu157=
NM_000155.4:c.796G= MANE Select	NP_000146.2:p.Glu266=
NM_001258332.2:c.469G=	NP_001245261.1:p.Glu157=