Canonical Allele Identifier: CA1845638832

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648397A= , CM000671.2:g.34648397A=	GRCh38
NC_000009.11:g.34648394A= , CM000671.1:g.34648394A=	GRCh37
NC_000009.10:g.34638394A=	NCBI36
NG_009029.1:g.6760A=
NG_028966.1:g.1213A=
NG_009029.2:g.6809A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*216A=	ENSP00000509954.1:n.*216A=
ENST00000378842.8:c.628A= MANE Select	ENSP00000368119.4:p.Lys210=
ENST00000378842.7:c.628A=	ENSP00000368119.3:p.Lys210=
ENST00000450095.6:c.301A=	ENSP00000401956.2:p.Lys101=
ENST00000472111.5:n.884A=
ENST00000473506.6:c.*216A=	ENSP00000432839.2:n.*216A=
ENST00000473529.5:n.787A=
ENST00000487381.5:n.1013A=
ENST00000489643.6:n.403A=
ENST00000554085.5:c.*372A=	ENSP00000450419.1:n.*372A=
ENST00000554550.5:c.*248A=	ENSP00000451435.1:n.*248A=
ENST00000554638.5:n.1100A=
ENST00000555020.5:n.784A=
ENST00000555086.5:n.632A=
ENST00000555214.5:n.449A=
ENST00000556244.1:c.615A=
ENST00000556278.1:c.373A=	ENSP00000451792.1:p.Lys125=
ENST00000556494.5:n.749A=
ENST00000557706.5:n.1190A=
NM_000155.3:c.628A=	NP_000146.2:p.Lys210=
NM_001258332.1:c.301A=	NP_001245261.1:p.Lys101=
NM_000155.4:c.628A= MANE Select	NP_000146.2:p.Lys210=
NM_001258332.2:c.301A=	NP_001245261.1:p.Lys101=