Canonical Allele Identifier: CA1845635369

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647126G= , CM000671.2:g.34647126G=	GRCh38
NC_000009.11:g.34647123G= , CM000671.1:g.34647123G=	GRCh37
NC_000009.10:g.34637123G=	NCBI36
NG_009029.1:g.5489G=
NG_009029.2:g.5538G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.120G=	ENSP00000509954.1:p.Glu40=
ENST00000378842.8:c.120G= MANE Select	ENSP00000368119.4:p.Glu40=
ENST00000378842.7:c.120G=	ENSP00000368119.3:p.Glu40=
ENST00000450095.6:c.-83G=	ENSP00000401956.2:n.-83G=
ENST00000465543.6:n.459G=
ENST00000468099.2:n.160G=
ENST00000472111.5:n.161G=
ENST00000473506.6:c.120G=	ENSP00000432839.2:p.Glu40=
ENST00000473529.5:n.167G=
ENST00000485531.1:n.113G=
ENST00000487381.5:n.146G=
ENST00000489643.6:n.150G=
ENST00000554085.5:c.120G=	ENSP00000450419.1:p.Glu40=
ENST00000554139.5:n.173G=
ENST00000554330.5:n.117G=
ENST00000554550.5:c.120G=	ENSP00000451435.1:p.Glu40=
ENST00000554638.5:n.144G=
ENST00000554897.5:c.120G=	ENSP00000450942.1:p.Glu40=
ENST00000554944.5:n.150G=
ENST00000555020.5:n.150G=
ENST00000555086.5:n.124G=
ENST00000555214.5:n.129G=
ENST00000556157.1:n.227G=
ENST00000556244.1:c.4G=
ENST00000556278.1:c.120G=	ENSP00000451792.1:p.Glu40=
ENST00000556403.5:n.133G=
ENST00000556494.5:n.152G=
ENST00000557541.5:n.313G=
ENST00000557706.5:n.234G=
ENST00000605275.1:n.658G=
NM_000155.3:c.120G=	NP_000146.2:p.Glu40=
NM_001258332.1:c.-83G=	NP_001245261.1:n.-83G=
NM_000155.4:c.120G= MANE Select	NP_000146.2:p.Glu40=
NM_001258332.2:c.-83G=	NP_001245261.1:n.-83G=