Canonical Allele Identifier: CA1845638998

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648436C= , CM000671.2:g.34648436C=	GRCh38
NC_000009.11:g.34648433C= , CM000671.1:g.34648433C=	GRCh37
NC_000009.10:g.34638433C=	NCBI36
NG_009029.1:g.6799C=
NG_028966.1:g.1252C=
NG_009029.2:g.6848C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*255C=	ENSP00000509954.1:n.*255C=
ENST00000378842.8:c.667C= MANE Select	ENSP00000368119.4:p.Arg223=
ENST00000378842.7:c.667C=	ENSP00000368119.3:p.Arg223=
ENST00000450095.6:c.340C=	ENSP00000401956.2:p.Arg114=
ENST00000472111.5:n.923C=
ENST00000473506.6:c.*255C=	ENSP00000432839.2:n.*255C=
ENST00000473529.5:n.826C=
ENST00000487381.5:n.1052C=
ENST00000489643.6:n.442C=
ENST00000554085.5:c.*411C=	ENSP00000450419.1:n.*411C=
ENST00000554550.5:c.*287C=	ENSP00000451435.1:n.*287C=
ENST00000554638.5:n.1139C=
ENST00000555020.5:n.823C=
ENST00000555086.5:n.671C=
ENST00000555214.5:n.488C=
ENST00000555754.1:n.12C=
ENST00000556244.1:c.654C=
ENST00000556278.1:c.412C=	ENSP00000451792.1:p.Arg138=
ENST00000556494.5:n.788C=
ENST00000557706.5:n.1229C=
NM_000155.3:c.667C=	NP_000146.2:p.Arg223=
NM_001258332.1:c.340C=	NP_001245261.1:p.Arg114=
NM_000155.4:c.667C= MANE Select	NP_000146.2:p.Arg223=
NM_001258332.2:c.340C=	NP_001245261.1:p.Arg114=