Canonical Allele Identifier: CA1584763498

Gene: LECT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135952958C= , CM000667.2:g.135952958C=	GRCh38
NC_000005.9:g.135288647C= , CM000667.1:g.135288647C=	GRCh37
NC_000005.8:g.135316546C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000274507.6:c.56G= MANE Select	ENSP00000274507.1:p.Gly19=
ENST00000274507.5:c.56G=	ENSP00000274507.1:p.Gly19=
ENST00000471827.1:n.159G=
ENST00000512872.1:c.-161G=	ENSP00000427012.1:n.-161G=
ENST00000514447.2:c.56G=	ENSP00000421123.2:p.Gly19=
ENST00000522943.5:c.56G=	ENSP00000429618.1:p.Gly19=
NM_002302.2:c.56G=	NP_002293.2:p.Gly19=
NM_002302.3:c.56G= MANE Select	NP_002293.2:p.Gly19=