Canonical Allele Identifier: CA1845638319

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648211T= , CM000671.2:g.34648211T=	GRCh38
NC_000009.11:g.34648208T= , CM000671.1:g.34648208T=	GRCh37
NC_000009.10:g.34638208T=	NCBI36
NG_009029.1:g.6574T=
NG_028966.1:g.1027T=
NG_009029.2:g.6623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*152+40T=	ENSP00000509954.1:n.*152+40T=
ENST00000378842.8:c.564+40T= MANE Select	ENSP00000368119.4:n.564+40T=
ENST00000378842.7:c.564+40T=	ENSP00000368119.3:n.564+40T=
ENST00000450095.6:c.237+40T=	ENSP00000401956.2:n.237+40T=
ENST00000472111.5:n.820+40T=
ENST00000473506.6:c.*152+40T=	ENSP00000432839.2:n.*152+40T=
ENST00000473529.5:n.723+40T=
ENST00000485531.1:n.1158+40T=
ENST00000487381.5:n.949+40T=
ENST00000489643.6:n.339+40T=
ENST00000554085.5:c.*308+40T=	ENSP00000450419.1:n.*308+40T=
ENST00000554139.5:n.810+40T=
ENST00000554550.5:c.*184+40T=	ENSP00000451435.1:n.*184+40T=
ENST00000554638.5:n.1036+40T=
ENST00000554897.5:c.*251+40T=	ENSP00000450942.1:n.*251+40T=
ENST00000554944.5:n.913+40T=
ENST00000555020.5:n.720+40T=
ENST00000555086.5:n.568+40T=
ENST00000555214.5:n.385+40T=
ENST00000556244.1:c.551+40T=
ENST00000556278.1:c.309+40T=	ENSP00000451792.1:n.309+40T=
ENST00000556494.5:n.685+40T=
ENST00000557706.5:n.1126+40T=
NM_000155.3:c.564+40T=	NP_000146.2:n.564+40T=
NM_001258332.1:c.237+40T=	NP_001245261.1:n.237+40T=
NM_000155.4:c.564+40T= MANE Select	NP_000146.2:n.564+40T=
NM_001258332.2:c.237+40T=	NP_001245261.1:n.237+40T=