Canonical Allele Identifier: CA1845638715

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648374A= , CM000671.2:g.34648374A=	GRCh38
NC_000009.11:g.34648371A= , CM000671.1:g.34648371A=	GRCh37
NC_000009.10:g.34638371A=	NCBI36
NG_009029.1:g.6737A=
NG_028966.1:g.1190A=
NG_009029.2:g.6786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*193A=	ENSP00000509954.1:n.*193A=
ENST00000378842.8:c.605A= MANE Select	ENSP00000368119.4:p.Glu202=
ENST00000378842.7:c.605A=	ENSP00000368119.3:p.Glu202=
ENST00000450095.6:c.278A=	ENSP00000401956.2:p.Glu93=
ENST00000472111.5:n.861A=
ENST00000473506.6:c.*193A=	ENSP00000432839.2:n.*193A=
ENST00000473529.5:n.764A=
ENST00000485531.1:n.1199A=
ENST00000487381.5:n.990A=
ENST00000489643.6:n.380A=
ENST00000554085.5:c.*349A=	ENSP00000450419.1:n.*349A=
ENST00000554139.5:n.851A=
ENST00000554550.5:c.*225A=	ENSP00000451435.1:n.*225A=
ENST00000554638.5:n.1077A=
ENST00000554897.5:c.*292A=	ENSP00000450942.1:n.*292A=
ENST00000554944.5:n.954A=
ENST00000555020.5:n.761A=
ENST00000555086.5:n.609A=
ENST00000555214.5:n.426A=
ENST00000556244.1:c.592A=
ENST00000556278.1:c.350A=	ENSP00000451792.1:p.Glu117=
ENST00000556494.5:n.726A=
ENST00000557706.5:n.1167A=
NM_000155.3:c.605A=	NP_000146.2:p.Glu202=
NM_001258332.1:c.278A=	NP_001245261.1:p.Glu93=
NM_000155.4:c.605A= MANE Select	NP_000146.2:p.Glu202=
NM_001258332.2:c.278A=	NP_001245261.1:p.Glu93=