Canonical Allele Identifier: CA1584763500
Gene: LECT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952962C= , CM000667.2:g.135952962C= GRCh38
NC_000005.9:g.135288651C= , CM000667.1:g.135288651C= GRCh37
NC_000005.8:g.135316550C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274507.6:c.52G= MANE Select ENSP00000274507.1:p.Ala18=
ENST00000274507.5:c.52G= ENSP00000274507.1:p.Ala18=
ENST00000471827.1:n.155G=
ENST00000512872.1:c.-165G= ENSP00000427012.1:n.-165G=
ENST00000514447.2:c.52G= ENSP00000421123.2:p.Ala18=
ENST00000522943.5:c.52G= ENSP00000429618.1:p.Ala18=
NM_002302.2:c.52G= NP_002293.2:p.Ala18=
NM_002302.3:c.52G= MANE Select NP_002293.2:p.Ala18=