Canonical Allele Identifier: CA1845635438

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647145C= , CM000671.2:g.34647145C=	GRCh38
NC_000009.11:g.34647142C= , CM000671.1:g.34647142C=	GRCh37
NC_000009.10:g.34637142C=	NCBI36
NG_009029.1:g.5508C=
NG_009029.2:g.5557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.139C=	ENSP00000509954.1:p.His47=
ENST00000378842.8:c.139C= MANE Select	ENSP00000368119.4:p.His47=
ENST00000378842.7:c.139C=	ENSP00000368119.3:p.His47=
ENST00000450095.6:c.-64C=	ENSP00000401956.2:n.-64C=
ENST00000465543.6:n.478C=
ENST00000468099.2:n.179C=
ENST00000472111.5:n.180C=
ENST00000473506.6:c.139C=	ENSP00000432839.2:p.His47=
ENST00000473529.5:n.186C=
ENST00000485531.1:n.132C=
ENST00000487381.5:n.165C=
ENST00000489643.6:n.169C=
ENST00000554085.5:c.139C=	ENSP00000450419.1:p.His47=
ENST00000554139.5:n.192C=
ENST00000554330.5:n.136C=
ENST00000554550.5:c.139C=	ENSP00000451435.1:p.His47=
ENST00000554638.5:n.163C=
ENST00000554897.5:c.139C=	ENSP00000450942.1:p.His47=
ENST00000554944.5:n.169C=
ENST00000555020.5:n.169C=
ENST00000555086.5:n.143C=
ENST00000555214.5:n.148C=
ENST00000556157.1:n.246C=
ENST00000556244.1:c.23C=
ENST00000556278.1:c.139C=	ENSP00000451792.1:p.His47=
ENST00000556403.5:n.152C=
ENST00000556494.5:n.171C=
ENST00000557541.5:n.332C=
ENST00000557706.5:n.253C=
ENST00000605275.1:n.677C=
NM_000155.3:c.139C=	NP_000146.2:p.His47=
NM_001258332.1:c.-64C=	NP_001245261.1:n.-64C=
NM_000155.4:c.139C= MANE Select	NP_000146.2:p.His47=
NM_001258332.2:c.-64C=	NP_001245261.1:n.-64C=