Canonical Allele Identifier: CA1845638660

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648364G= , CM000671.2:g.34648364G=	GRCh38
NC_000009.11:g.34648361G= , CM000671.1:g.34648361G=	GRCh37
NC_000009.10:g.34638361G=	NCBI36
NG_009029.1:g.6727G=
NG_028966.1:g.1180G=
NG_009029.2:g.6776G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*183G=	ENSP00000509954.1:n.*183G=
ENST00000378842.8:c.595G= MANE Select	ENSP00000368119.4:p.Ala199=
ENST00000378842.7:c.595G=	ENSP00000368119.3:p.Ala199=
ENST00000450095.6:c.268G=	ENSP00000401956.2:p.Ala90=
ENST00000472111.5:n.851G=
ENST00000473506.6:c.*183G=	ENSP00000432839.2:n.*183G=
ENST00000473529.5:n.754G=
ENST00000485531.1:n.1189G=
ENST00000487381.5:n.980G=
ENST00000489643.6:n.370G=
ENST00000554085.5:c.*339G=	ENSP00000450419.1:n.*339G=
ENST00000554139.5:n.841G=
ENST00000554550.5:c.*215G=	ENSP00000451435.1:n.*215G=
ENST00000554638.5:n.1067G=
ENST00000554897.5:c.*282G=	ENSP00000450942.1:n.*282G=
ENST00000554944.5:n.944G=
ENST00000555020.5:n.751G=
ENST00000555086.5:n.599G=
ENST00000555214.5:n.416G=
ENST00000556244.1:c.582G=
ENST00000556278.1:c.340G=	ENSP00000451792.1:p.Ala114=
ENST00000556494.5:n.716G=
ENST00000557706.5:n.1157G=
NM_000155.3:c.595G=	NP_000146.2:p.Ala199=
NM_001258332.1:c.268G=	NP_001245261.1:p.Ala90=
NM_000155.4:c.595G= MANE Select	NP_000146.2:p.Ala199=
NM_001258332.2:c.268G=	NP_001245261.1:p.Ala90=