Canonical Allele Identifier: CA1845636759

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647748G= , CM000671.2:g.34647748G=	GRCh38
NC_000009.11:g.34647745G= , CM000671.1:g.34647745G=	GRCh37
NC_000009.10:g.34637745G=	NCBI36
NG_009029.1:g.6111G=
NG_028966.1:g.564G=
NG_009029.2:g.6160G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-84G=	ENSP00000509954.1:n.329-84G=
ENST00000378842.8:c.377+43G= MANE Select	ENSP00000368119.4:n.377+43G=
ENST00000378842.7:c.377+43G=	ENSP00000368119.3:n.377+43G=
ENST00000450095.6:c.51-84G=	ENSP00000401956.2:n.51-84G=
ENST00000465543.6:n.716+43G=
ENST00000472111.5:n.550G=
ENST00000473506.6:c.328+43G=	ENSP00000432839.2:n.328+43G=
ENST00000473529.5:n.513+43G=
ENST00000485531.1:n.735G=
ENST00000487381.5:n.679G=
ENST00000489643.6:n.283-367G=
ENST00000554085.5:c.*121+43G=	ENSP00000450419.1:n.*121+43G=
ENST00000554139.5:n.473G=
ENST00000554330.5:n.457G=
ENST00000554550.5:c.253-84G=	ENSP00000451435.1:n.253-84G=
ENST00000554638.5:n.766G=
ENST00000554897.5:c.253-84G=	ENSP00000450942.1:n.253-84G=
ENST00000554944.5:n.490G=
ENST00000555020.5:n.450G=
ENST00000555086.5:n.381+43G=
ENST00000555214.5:n.262-300G=
ENST00000556157.1:n.544G=
ENST00000556244.1:c.364+43G=
ENST00000556278.1:c.253-367G=	ENSP00000451792.1:n.253-367G=
ENST00000556403.5:n.522G=
ENST00000556494.5:n.498+43G=
ENST00000557541.5:n.521+43G=
ENST00000557706.5:n.856G=
NM_000155.3:c.377+43G=	NP_000146.2:n.377+43G=
NM_001258332.1:c.51-84G=	NP_001245261.1:n.51-84G=
NM_000155.4:c.377+43G= MANE Select	NP_000146.2:n.377+43G=
NM_001258332.2:c.51-84G=	NP_001245261.1:n.51-84G=