Canonical Allele Identifier: CA1845638723

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648376G= , CM000671.2:g.34648376G=	GRCh38
NC_000009.11:g.34648373G= , CM000671.1:g.34648373G=	GRCh37
NC_000009.10:g.34638373G=	NCBI36
NG_009029.1:g.6739G=
NG_028966.1:g.1192G=
NG_009029.2:g.6788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*195G=	ENSP00000509954.1:n.*195G=
ENST00000378842.8:c.607G= MANE Select	ENSP00000368119.4:p.Glu203=
ENST00000378842.7:c.607G=	ENSP00000368119.3:p.Glu203=
ENST00000450095.6:c.280G=	ENSP00000401956.2:p.Glu94=
ENST00000472111.5:n.863G=
ENST00000473506.6:c.*195G=	ENSP00000432839.2:n.*195G=
ENST00000473529.5:n.766G=
ENST00000485531.1:n.1201G=
ENST00000487381.5:n.992G=
ENST00000489643.6:n.382G=
ENST00000554085.5:c.*351G=	ENSP00000450419.1:n.*351G=
ENST00000554139.5:n.853G=
ENST00000554550.5:c.*227G=	ENSP00000451435.1:n.*227G=
ENST00000554638.5:n.1079G=
ENST00000554944.5:n.956G=
ENST00000555020.5:n.763G=
ENST00000555086.5:n.611G=
ENST00000555214.5:n.428G=
ENST00000556244.1:c.594G=
ENST00000556278.1:c.352G=	ENSP00000451792.1:p.Glu118=
ENST00000556494.5:n.728G=
ENST00000557706.5:n.1169G=
NM_000155.3:c.607G=	NP_000146.2:p.Glu203=
NM_001258332.1:c.280G=	NP_001245261.1:p.Glu94=
NM_000155.4:c.607G= MANE Select	NP_000146.2:p.Glu203=
NM_001258332.2:c.280G=	NP_001245261.1:p.Glu94=