Canonical Allele Identifier: CA1845641493

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649503G= , CM000671.2:g.34649503G=	GRCh38
NC_000009.11:g.34649500G= , CM000671.1:g.34649500G=	GRCh37
NC_000009.10:g.34639500G=	NCBI36
NG_009029.1:g.7866G=
NG_028966.1:g.2319G=
NG_009029.2:g.7915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*586G=	ENSP00000509954.1:n.*586G=
ENST00000378842.8:c.998G= MANE Select	ENSP00000368119.4:p.Arg333=
ENST00000378842.7:c.998G=	ENSP00000368119.3:p.Arg333=
ENST00000450095.6:c.671G=	ENSP00000401956.2:p.Arg224=
ENST00000488412.2:n.582G=
ENST00000489643.6:n.1406G=
ENST00000554550.5:c.*618G=	ENSP00000451435.1:n.*618G=
ENST00000554638.5:n.1470G=
ENST00000555020.5:n.1787G=
ENST00000555754.1:n.446G=
ENST00000556278.1:c.432+1047G=	ENSP00000451792.1:n.432+1047G=
ENST00000557706.5:n.1573G=
NM_000155.3:c.998G=	NP_000146.2:p.Arg333=
NM_001258332.1:c.671G=	NP_001245261.1:p.Arg224=
NM_000155.4:c.998G= MANE Select	NP_000146.2:p.Arg333=
NM_001258332.2:c.671G=	NP_001245261.1:p.Arg224=