Canonical Allele Identifier: CA1845638363

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648249G= , CM000671.2:g.34648249G=	GRCh38
NC_000009.11:g.34648246G= , CM000671.1:g.34648246G=	GRCh37
NC_000009.10:g.34638246G=	NCBI36
NG_009029.1:g.6612G=
NG_028966.1:g.1065G=
NG_009029.2:g.6661G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*152+78G=	ENSP00000509954.1:n.*152+78G=
ENST00000378842.8:c.564+78G= MANE Select	ENSP00000368119.4:n.564+78G=
ENST00000378842.7:c.564+78G=	ENSP00000368119.3:n.564+78G=
ENST00000450095.6:c.237+78G=	ENSP00000401956.2:n.237+78G=
ENST00000472111.5:n.820+78G=
ENST00000473506.6:c.*152+78G=	ENSP00000432839.2:n.*152+78G=
ENST00000473529.5:n.723+78G=
ENST00000485531.1:n.1158+78G=
ENST00000487381.5:n.949+78G=
ENST00000489643.6:n.339+78G=
ENST00000554085.5:c.*308+78G=	ENSP00000450419.1:n.*308+78G=
ENST00000554139.5:n.810+78G=
ENST00000554550.5:c.*184+78G=	ENSP00000451435.1:n.*184+78G=
ENST00000554638.5:n.1036+78G=
ENST00000554897.5:c.*251+78G=	ENSP00000450942.1:n.*251+78G=
ENST00000554944.5:n.913+78G=
ENST00000555020.5:n.720+78G=
ENST00000555086.5:n.568+78G=
ENST00000555214.5:n.385+78G=
ENST00000556244.1:c.551+78G=
ENST00000556278.1:c.309+78G=	ENSP00000451792.1:n.309+78G=
ENST00000556494.5:n.685+78G=
ENST00000557706.5:n.1126+78G=
NM_000155.3:c.564+78G=	NP_000146.2:n.564+78G=
NM_001258332.1:c.237+78G=	NP_001245261.1:n.237+78G=
NM_000155.4:c.564+78G= MANE Select	NP_000146.2:n.564+78G=
NM_001258332.2:c.237+78G=	NP_001245261.1:n.237+78G=