Canonical Allele Identifier: CA1845636988

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647844C= , CM000671.2:g.34647844C=	GRCh38
NC_000009.11:g.34647841C= , CM000671.1:g.34647841C=	GRCh37
NC_000009.10:g.34637841C=	NCBI36
NG_009029.1:g.6207C=
NG_028966.1:g.660C=
NG_009029.2:g.6256C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.341C=	ENSP00000509954.1:p.Ala114=
ENST00000378842.8:c.390C= MANE Select	ENSP00000368119.4:p.Cys130=
ENST00000378842.7:c.390C=	ENSP00000368119.3:p.Cys130=
ENST00000450095.6:c.63C=	ENSP00000401956.2:p.Cys21=
ENST00000465543.6:n.729C=
ENST00000472111.5:n.646C=
ENST00000473506.6:c.341C=	ENSP00000432839.2:p.Ala114=
ENST00000473529.5:n.526C=
ENST00000485531.1:n.831C=
ENST00000487381.5:n.775C=
ENST00000489643.6:n.283-271C=
ENST00000554085.5:c.*134C=	ENSP00000450419.1:n.*134C=
ENST00000554139.5:n.569C=
ENST00000554330.5:n.553C=
ENST00000554550.5:c.*10C=	ENSP00000451435.1:n.*10C=
ENST00000554638.5:n.862C=
ENST00000554897.5:c.*10C=	ENSP00000450942.1:n.*10C=
ENST00000554944.5:n.586C=
ENST00000555020.5:n.546C=
ENST00000555086.5:n.394C=
ENST00000555214.5:n.262-204C=
ENST00000556244.1:c.377C=
ENST00000556278.1:c.253-271C=	ENSP00000451792.1:n.253-271C=
ENST00000556494.5:n.511C=
ENST00000557541.5:n.534C=
ENST00000557706.5:n.952C=
NM_000155.3:c.390C=	NP_000146.2:p.Cys130=
NM_001258332.1:c.63C=	NP_001245261.1:p.Cys21=
NM_000155.4:c.390C= MANE Select	NP_000146.2:p.Cys130=
NM_001258332.2:c.63C=	NP_001245261.1:p.Cys21=