Canonical Allele Identifier: CA1845636778

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647754T= , CM000671.2:g.34647754T=	GRCh38
NC_000009.11:g.34647751T= , CM000671.1:g.34647751T=	GRCh37
NC_000009.10:g.34637751T=	NCBI36
NG_009029.1:g.6117T=
NG_028966.1:g.570T=
NG_009029.2:g.6166T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-78T=	ENSP00000509954.1:n.329-78T=
ENST00000378842.8:c.377+49T= MANE Select	ENSP00000368119.4:n.377+49T=
ENST00000378842.7:c.377+49T=	ENSP00000368119.3:n.377+49T=
ENST00000450095.6:c.51-78T=	ENSP00000401956.2:n.51-78T=
ENST00000465543.6:n.716+49T=
ENST00000472111.5:n.556T=
ENST00000473506.6:c.328+49T=	ENSP00000432839.2:n.328+49T=
ENST00000473529.5:n.513+49T=
ENST00000485531.1:n.741T=
ENST00000487381.5:n.685T=
ENST00000489643.6:n.283-361T=
ENST00000554085.5:c.*121+49T=	ENSP00000450419.1:n.*121+49T=
ENST00000554139.5:n.479T=
ENST00000554330.5:n.463T=
ENST00000554550.5:c.253-78T=	ENSP00000451435.1:n.253-78T=
ENST00000554638.5:n.772T=
ENST00000554897.5:c.253-78T=	ENSP00000450942.1:n.253-78T=
ENST00000554944.5:n.496T=
ENST00000555020.5:n.456T=
ENST00000555086.5:n.381+49T=
ENST00000555214.5:n.262-294T=
ENST00000556157.1:n.550T=
ENST00000556244.1:c.364+49T=
ENST00000556278.1:c.253-361T=	ENSP00000451792.1:n.253-361T=
ENST00000556403.5:n.528T=
ENST00000556494.5:n.498+49T=
ENST00000557541.5:n.521+49T=
ENST00000557706.5:n.862T=
NM_000155.3:c.377+49T=	NP_000146.2:n.377+49T=
NM_001258332.1:c.51-78T=	NP_001245261.1:n.51-78T=
NM_000155.4:c.377+49T= MANE Select	NP_000146.2:n.377+49T=
NM_001258332.2:c.51-78T=	NP_001245261.1:n.51-78T=