Canonical Allele Identifier: CA1845637834

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648077T= , CM000671.2:g.34648077T=	GRCh38
NC_000009.11:g.34648074T= , CM000671.1:g.34648074T=	GRCh37
NC_000009.10:g.34638074T=	NCBI36
NG_009029.1:g.6440T=
NG_028966.1:g.893T=
NG_009029.2:g.6489T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*96-38T=	ENSP00000509954.1:n.*96-38T=
ENST00000378842.8:c.508-38T= MANE Select	ENSP00000368119.4:n.508-38T=
ENST00000378842.7:c.508-38T=	ENSP00000368119.3:n.508-38T=
ENST00000450095.6:c.181-38T=	ENSP00000401956.2:n.181-38T=
ENST00000465543.6:n.847-38T=
ENST00000472111.5:n.764-38T=
ENST00000473506.6:c.*96-38T=	ENSP00000432839.2:n.*96-38T=
ENST00000473529.5:n.644-15T=
ENST00000485531.1:n.1064T=
ENST00000487381.5:n.893-38T=
ENST00000489643.6:n.283-38T=
ENST00000554085.5:c.*252-38T=	ENSP00000450419.1:n.*252-38T=
ENST00000554139.5:n.716T=
ENST00000554550.5:c.*128-38T=	ENSP00000451435.1:n.*128-38T=
ENST00000554638.5:n.980-38T=
ENST00000554897.5:c.*157T=	ENSP00000450942.1:n.*157T=
ENST00000554944.5:n.819T=
ENST00000555020.5:n.664-38T=
ENST00000555086.5:n.512-38T=
ENST00000555214.5:n.291T=
ENST00000556244.1:c.495-38T=
ENST00000556278.1:c.253-38T=	ENSP00000451792.1:n.253-38T=
ENST00000556494.5:n.629-38T=
ENST00000557706.5:n.1070-38T=
NM_000155.3:c.508-38T=	NP_000146.2:n.508-38T=
NM_001258332.1:c.181-38T=	NP_001245261.1:n.181-38T=
NM_000155.4:c.508-38T= MANE Select	NP_000146.2:n.508-38T=
NM_001258332.2:c.181-38T=	NP_001245261.1:n.181-38T=