Canonical Allele Identifier: CA1845635544

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647171T= , CM000671.2:g.34647171T=	GRCh38
NC_000009.11:g.34647168T= , CM000671.1:g.34647168T=	GRCh37
NC_000009.10:g.34637168T=	NCBI36
NG_009029.1:g.5534T=
NG_009029.2:g.5583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.165T=	ENSP00000509954.1:p.Gly55=
ENST00000378842.8:c.165T= MANE Select	ENSP00000368119.4:p.Gly55=
ENST00000378842.7:c.165T=	ENSP00000368119.3:p.Gly55=
ENST00000450095.6:c.-38T=	ENSP00000401956.2:n.-38T=
ENST00000465543.6:n.504T=
ENST00000468099.2:n.205T=
ENST00000472111.5:n.206T=
ENST00000473506.6:c.165T=	ENSP00000432839.2:p.Gly55=
ENST00000473529.5:n.212T=
ENST00000485531.1:n.158T=
ENST00000487381.5:n.191T=
ENST00000489643.6:n.195T=
ENST00000554085.5:c.165T=	ENSP00000450419.1:p.Gly55=
ENST00000554139.5:n.218T=
ENST00000554330.5:n.162T=
ENST00000554550.5:c.165T=	ENSP00000451435.1:p.Gly55=
ENST00000554638.5:n.189T=
ENST00000554897.5:c.165T=	ENSP00000450942.1:p.Gly55=
ENST00000554944.5:n.195T=
ENST00000555020.5:n.195T=
ENST00000555086.5:n.169T=
ENST00000555214.5:n.174T=
ENST00000556157.1:n.272T=
ENST00000556244.1:c.49T=
ENST00000556278.1:c.165T=	ENSP00000451792.1:p.Gly55=
ENST00000556403.5:n.178T=
ENST00000556494.5:n.197T=
ENST00000557541.5:n.358T=
ENST00000557706.5:n.279T=
NM_000155.3:c.165T=	NP_000146.2:p.Gly55=
NM_001258332.1:c.-38T=	NP_001245261.1:n.-38T=
NM_000155.4:c.165T= MANE Select	NP_000146.2:p.Gly55=
NM_001258332.2:c.-38T=	NP_001245261.1:n.-38T=