Canonical Allele Identifier: CA1845638009

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648131G= , CM000671.2:g.34648131G=	GRCh38
NC_000009.11:g.34648128G= , CM000671.1:g.34648128G=	GRCh37
NC_000009.10:g.34638128G=	NCBI36
NG_009029.1:g.6494G=
NG_028966.1:g.947G=
NG_009029.2:g.6543G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*112G=	ENSP00000509954.1:n.*112G=
ENST00000378842.8:c.524G= MANE Select	ENSP00000368119.4:p.Gly175=
ENST00000378842.7:c.524G=	ENSP00000368119.3:p.Gly175=
ENST00000450095.6:c.197G=	ENSP00000401956.2:p.Gly66=
ENST00000465543.6:n.863G=
ENST00000472111.5:n.780G=
ENST00000473506.6:c.*112G=	ENSP00000432839.2:n.*112G=
ENST00000473529.5:n.683G=
ENST00000485531.1:n.1118G=
ENST00000487381.5:n.909G=
ENST00000489643.6:n.299G=
ENST00000554085.5:c.*268G=	ENSP00000450419.1:n.*268G=
ENST00000554139.5:n.770G=
ENST00000554550.5:c.*144G=	ENSP00000451435.1:n.*144G=
ENST00000554638.5:n.996G=
ENST00000554897.5:c.*211G=	ENSP00000450942.1:n.*211G=
ENST00000554944.5:n.873G=
ENST00000555020.5:n.680G=
ENST00000555086.5:n.528G=
ENST00000555214.5:n.345G=
ENST00000556244.1:c.511G=
ENST00000556278.1:c.269G=	ENSP00000451792.1:p.Gly90=
ENST00000556494.5:n.645G=
ENST00000557706.5:n.1086G=
NM_000155.3:c.524G=	NP_000146.2:p.Gly175=
NM_001258332.1:c.197G=	NP_001245261.1:p.Gly66=
NM_000155.4:c.524G= MANE Select	NP_000146.2:p.Gly175=
NM_001258332.2:c.197G=	NP_001245261.1:p.Gly66=