Canonical Allele Identifier: CA1845636806

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647775G= , CM000671.2:g.34647775G=	GRCh38
NC_000009.11:g.34647772G= , CM000671.1:g.34647772G=	GRCh37
NC_000009.10:g.34637772G=	NCBI36
NG_009029.1:g.6138G=
NG_028966.1:g.591G=
NG_009029.2:g.6187G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-57G=	ENSP00000509954.1:n.329-57G=
ENST00000378842.8:c.378-57G= MANE Select	ENSP00000368119.4:n.378-57G=
ENST00000378842.7:c.378-57G=	ENSP00000368119.3:n.378-57G=
ENST00000450095.6:c.51-57G=	ENSP00000401956.2:n.51-57G=
ENST00000465543.6:n.717-57G=
ENST00000472111.5:n.577G=
ENST00000473506.6:c.329-57G=	ENSP00000432839.2:n.329-57G=
ENST00000473529.5:n.514-57G=
ENST00000485531.1:n.762G=
ENST00000487381.5:n.706G=
ENST00000489643.6:n.283-340G=
ENST00000554085.5:c.*122-57G=	ENSP00000450419.1:n.*122-57G=
ENST00000554139.5:n.500G=
ENST00000554330.5:n.484G=
ENST00000554550.5:c.253-57G=	ENSP00000451435.1:n.253-57G=
ENST00000554638.5:n.793G=
ENST00000554897.5:c.253-57G=	ENSP00000450942.1:n.253-57G=
ENST00000554944.5:n.517G=
ENST00000555020.5:n.477G=
ENST00000555086.5:n.382-57G=
ENST00000555214.5:n.262-273G=
ENST00000556244.1:c.365-57G=
ENST00000556278.1:c.253-340G=	ENSP00000451792.1:n.253-340G=
ENST00000556403.5:n.549G=
ENST00000556494.5:n.499-57G=
ENST00000557541.5:n.522-57G=
ENST00000557706.5:n.883G=
NM_000155.3:c.378-57G=	NP_000146.2:n.378-57G=
NM_001258332.1:c.51-57G=	NP_001245261.1:n.51-57G=
NM_000155.4:c.378-57G= MANE Select	NP_000146.2:n.378-57G=
NM_001258332.2:c.51-57G=	NP_001245261.1:n.51-57G=