Canonical Allele Identifier: CA1845636979

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647843G= , CM000671.2:g.34647843G=	GRCh38
NC_000009.11:g.34647840G= , CM000671.1:g.34647840G=	GRCh37
NC_000009.10:g.34637840G=	NCBI36
NG_009029.1:g.6206G=
NG_028966.1:g.659G=
NG_009029.2:g.6255G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.340G=	ENSP00000509954.1:p.Ala114=
ENST00000378842.8:c.389G= MANE Select	ENSP00000368119.4:p.Cys130=
ENST00000378842.7:c.389G=	ENSP00000368119.3:p.Cys130=
ENST00000450095.6:c.62G=	ENSP00000401956.2:p.Cys21=
ENST00000465543.6:n.728G=
ENST00000472111.5:n.645G=
ENST00000473506.6:c.340G=	ENSP00000432839.2:p.Ala114=
ENST00000473529.5:n.525G=
ENST00000485531.1:n.830G=
ENST00000487381.5:n.774G=
ENST00000489643.6:n.283-272G=
ENST00000554085.5:c.*133G=	ENSP00000450419.1:n.*133G=
ENST00000554139.5:n.568G=
ENST00000554330.5:n.552G=
ENST00000554550.5:c.*9G=	ENSP00000451435.1:n.*9G=
ENST00000554638.5:n.861G=
ENST00000554897.5:c.*9G=	ENSP00000450942.1:n.*9G=
ENST00000554944.5:n.585G=
ENST00000555020.5:n.545G=
ENST00000555086.5:n.393G=
ENST00000555214.5:n.262-205G=
ENST00000556244.1:c.376G=
ENST00000556278.1:c.253-272G=	ENSP00000451792.1:n.253-272G=
ENST00000556494.5:n.510G=
ENST00000557541.5:n.533G=
ENST00000557706.5:n.951G=
NM_000155.3:c.389G=	NP_000146.2:p.Cys130=
NM_001258332.1:c.62G=	NP_001245261.1:p.Cys21=
NM_000155.4:c.389G= MANE Select	NP_000146.2:p.Cys130=
NM_001258332.2:c.62G=	NP_001245261.1:p.Cys21=