Canonical Allele Identifier: CA1845639886

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648859G= , CM000671.2:g.34648859G=	GRCh38
NC_000009.11:g.34648856G= , CM000671.1:g.34648856G=	GRCh37
NC_000009.10:g.34638856G=	NCBI36
NG_009029.1:g.7222G=
NG_028966.1:g.1675G=
NG_009029.2:g.7271G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*373G=	ENSP00000509954.1:n.*373G=
ENST00000378842.8:c.785G= MANE Select	ENSP00000368119.4:p.Arg262=
ENST00000378842.7:c.785G=	ENSP00000368119.3:p.Arg262=
ENST00000450095.6:c.458G=	ENSP00000401956.2:p.Arg153=
ENST00000473506.6:c.*373G=	ENSP00000432839.2:n.*373G=
ENST00000489643.6:n.865G=
ENST00000554085.5:c.*529G=	ENSP00000450419.1:n.*529G=
ENST00000554550.5:c.*405G=	ENSP00000451435.1:n.*405G=
ENST00000554638.5:n.1257G=
ENST00000555020.5:n.1246G=
ENST00000555086.5:n.789G=
ENST00000555754.1:n.130G=
ENST00000556244.1:c.772G=
ENST00000556278.1:c.432+403G=	ENSP00000451792.1:n.432+403G=
ENST00000557706.5:n.1347G=
NM_000155.3:c.785G=	NP_000146.2:p.Arg262=
NM_001258332.1:c.458G=	NP_001245261.1:p.Arg153=
NM_000155.4:c.785G= MANE Select	NP_000146.2:p.Arg262=
NM_001258332.2:c.458G=	NP_001245261.1:p.Arg153=