Canonical Allele Identifier: CA1845639601

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648776A= , CM000671.2:g.34648776A=	GRCh38
NC_000009.11:g.34648773A= , CM000671.1:g.34648773A=	GRCh37
NC_000009.10:g.34638773A=	NCBI36
NG_009029.1:g.7139A=
NG_028966.1:g.1592A=
NG_009029.2:g.7188A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*290A=	ENSP00000509954.1:n.*290A=
ENST00000378842.8:c.702A= MANE Select	ENSP00000368119.4:p.Leu234=
ENST00000378842.7:c.702A=	ENSP00000368119.3:p.Leu234=
ENST00000450095.6:c.375A=	ENSP00000401956.2:p.Leu125=
ENST00000473506.6:c.*290A=	ENSP00000432839.2:n.*290A=
ENST00000473529.5:n.861A=
ENST00000487381.5:n.1392A=
ENST00000489643.6:n.782A=
ENST00000554085.5:c.*446A=	ENSP00000450419.1:n.*446A=
ENST00000554550.5:c.*322A=	ENSP00000451435.1:n.*322A=
ENST00000554638.5:n.1174A=
ENST00000555020.5:n.1163A=
ENST00000555086.5:n.706A=
ENST00000555754.1:n.47A=
ENST00000556244.1:c.689A=
ENST00000556278.1:c.432+320A=	ENSP00000451792.1:n.432+320A=
ENST00000557706.5:n.1264A=
NM_000155.3:c.702A=	NP_000146.2:p.Leu234=
NM_001258332.1:c.375A=	NP_001245261.1:p.Leu125=
NM_000155.4:c.702A= MANE Select	NP_000146.2:p.Leu234=
NM_001258332.2:c.375A=	NP_001245261.1:p.Leu125=