Canonical Allele Identifier: CA1845636270

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647531G= , CM000671.2:g.34647531G=	GRCh38
NC_000009.11:g.34647528G= , CM000671.1:g.34647528G=	GRCh37
NC_000009.10:g.34637528G=	NCBI36
NG_009029.1:g.5894G=
NG_028966.1:g.347G=
NG_009029.2:g.5943G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.292G=	ENSP00000509954.1:p.Asp98=
ENST00000378842.8:c.292G= MANE Select	ENSP00000368119.4:p.Asp98=
ENST00000378842.7:c.292G=	ENSP00000368119.3:p.Asp98=
ENST00000450095.6:c.50+273G=	ENSP00000401956.2:n.50+273G=
ENST00000465543.6:n.631G=
ENST00000472111.5:n.333G=
ENST00000473506.6:c.253-10G=	ENSP00000432839.2:n.253-10G=
ENST00000473529.5:n.339G=
ENST00000485531.1:n.518G=
ENST00000487381.5:n.551G=
ENST00000489643.6:n.282+273G=
ENST00000554085.5:c.*36G=	ENSP00000450419.1:n.*36G=
ENST00000554139.5:n.345G=
ENST00000554330.5:n.250-10G=
ENST00000554550.5:c.252+273G=	ENSP00000451435.1:n.252+273G=
ENST00000554638.5:n.549G=
ENST00000554897.5:c.252+273G=	ENSP00000450942.1:n.252+273G=
ENST00000554944.5:n.283-10G=
ENST00000555020.5:n.322G=
ENST00000555086.5:n.296G=
ENST00000555214.5:n.261+273G=
ENST00000556157.1:n.416G=
ENST00000556244.1:c.279G=
ENST00000556278.1:c.252+273G=	ENSP00000451792.1:n.252+273G=
ENST00000556403.5:n.305G=
ENST00000556494.5:n.324G=
ENST00000557541.5:n.446-10G=
ENST00000557706.5:n.639G=
NM_000155.3:c.292G=	NP_000146.2:p.Asp98=
NM_001258332.1:c.50+273G=	NP_001245261.1:n.50+273G=
NM_000155.4:c.292G= MANE Select	NP_000146.2:p.Asp98=
NM_001258332.2:c.50+273G=	NP_001245261.1:n.50+273G=