Canonical Allele Identifier: CA1845640507

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649053G= , CM000671.2:g.34649053G=	GRCh38
NC_000009.11:g.34649050G= , CM000671.1:g.34649050G=	GRCh37
NC_000009.10:g.34639050G=	NCBI36
NG_009029.1:g.7416G=
NG_028966.1:g.1869G=
NG_009029.2:g.7465G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*464G=	ENSP00000509954.1:n.*464G=
ENST00000378842.8:c.876G= MANE Select	ENSP00000368119.4:p.Thr292=
ENST00000378842.7:c.876G=	ENSP00000368119.3:p.Thr292=
ENST00000450095.6:c.549G=	ENSP00000401956.2:p.Thr183=
ENST00000488412.2:n.132G=
ENST00000489643.6:n.956G=
ENST00000554550.5:c.*496G=	ENSP00000451435.1:n.*496G=
ENST00000554638.5:n.1348G=
ENST00000555020.5:n.1337G=
ENST00000555086.5:n.983G=
ENST00000555754.1:n.324G=
ENST00000556278.1:c.432+597G=	ENSP00000451792.1:n.432+597G=
ENST00000557706.5:n.1451G=
NM_000155.3:c.876G=	NP_000146.2:p.Thr292=
NM_001258332.1:c.549G=	NP_001245261.1:p.Thr183=
NM_000155.4:c.876G= MANE Select	NP_000146.2:p.Thr292=
NM_001258332.2:c.549G=	NP_001245261.1:p.Thr183=