Canonical Allele Identifier: CA1845635312

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647106T= , CM000671.2:g.34647106T=	GRCh38
NC_000009.11:g.34647103T= , CM000671.1:g.34647103T=	GRCh37
NC_000009.10:g.34637103T=	NCBI36
NG_009029.1:g.5469T=
NG_009029.2:g.5518T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.100T=	ENSP00000509954.1:p.Tyr34=
ENST00000378842.8:c.100T= MANE Select	ENSP00000368119.4:p.Tyr34=
ENST00000378842.7:c.100T=	ENSP00000368119.3:p.Tyr34=
ENST00000450095.6:c.-103T=	ENSP00000401956.2:n.-103T=
ENST00000465543.6:n.439T=
ENST00000468099.2:n.155-15T=
ENST00000472111.5:n.141T=
ENST00000473506.6:c.100T=	ENSP00000432839.2:p.Tyr34=
ENST00000473529.5:n.147T=
ENST00000485531.1:n.93T=
ENST00000487381.5:n.126T=
ENST00000489643.6:n.130T=
ENST00000554085.5:c.100T=	ENSP00000450419.1:p.Tyr34=
ENST00000554139.5:n.153T=
ENST00000554330.5:n.97T=
ENST00000554550.5:c.100T=	ENSP00000451435.1:p.Tyr34=
ENST00000554638.5:n.124T=
ENST00000554897.5:c.100T=	ENSP00000450942.1:p.Tyr34=
ENST00000554944.5:n.130T=
ENST00000555020.5:n.130T=
ENST00000555086.5:n.104T=
ENST00000555214.5:n.109T=
ENST00000556157.1:n.207T=
ENST00000556278.1:c.100T=	ENSP00000451792.1:p.Tyr34=
ENST00000556403.5:n.113T=
ENST00000556494.5:n.132T=
ENST00000557541.5:n.293T=
ENST00000557706.5:n.214T=
ENST00000605275.1:n.638T=
NM_000155.3:c.100T=	NP_000146.2:p.Tyr34=
NM_001258332.1:c.-103T=	NP_001245261.1:n.-103T=
NM_000155.4:c.100T= MANE Select	NP_000146.2:p.Tyr34=
NM_001258332.2:c.-103T=	NP_001245261.1:n.-103T=