Canonical Allele Identifier: CA1845635651

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647200T= , CM000671.2:g.34647200T=	GRCh38
NC_000009.11:g.34647197T= , CM000671.1:g.34647197T=	GRCh37
NC_000009.10:g.34637197T=	NCBI36
NG_009029.1:g.5563T=
NG_028966.1:g.16T=
NG_009029.2:g.5612T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.194T=	ENSP00000509954.1:p.Val65=
ENST00000378842.8:c.194T= MANE Select	ENSP00000368119.4:p.Val65=
ENST00000378842.7:c.194T=	ENSP00000368119.3:p.Val65=
ENST00000450095.6:c.-9T=	ENSP00000401956.2:n.-9T=
ENST00000465543.6:n.533T=
ENST00000468099.2:n.234T=
ENST00000472111.5:n.235T=
ENST00000473506.6:c.194T=	ENSP00000432839.2:p.Val65=
ENST00000473529.5:n.241T=
ENST00000485531.1:n.187T=
ENST00000487381.5:n.220T=
ENST00000489643.6:n.224T=
ENST00000554085.5:c.194T=	ENSP00000450419.1:p.Val65=
ENST00000554139.5:n.247T=
ENST00000554330.5:n.191T=
ENST00000554550.5:c.194T=	ENSP00000451435.1:p.Val65=
ENST00000554638.5:n.218T=
ENST00000554897.5:c.194T=	ENSP00000450942.1:p.Val65=
ENST00000554944.5:n.224T=
ENST00000555020.5:n.224T=
ENST00000555086.5:n.198T=
ENST00000555214.5:n.203T=
ENST00000556157.1:n.301T=
ENST00000556244.1:c.78T=
ENST00000556278.1:c.194T=	ENSP00000451792.1:p.Val65=
ENST00000556403.5:n.207T=
ENST00000556494.5:n.226T=
ENST00000557541.5:n.387T=
ENST00000557706.5:n.308T=
NM_000155.3:c.194T=	NP_000146.2:p.Val65=
NM_001258332.1:c.-9T=	NP_001245261.1:n.-9T=
NM_000155.4:c.194T= MANE Select	NP_000146.2:p.Val65=
NM_001258332.2:c.-9T=	NP_001245261.1:n.-9T=