Canonical Allele Identifier: CA1584763415
Gene: LECT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952799A= , CM000667.2:g.135952799A= GRCh38
NC_000005.9:g.135288488A= , CM000667.1:g.135288488A= GRCh37
NC_000005.8:g.135316387A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.143+72T= MANE Select ENSP00000274507.1:n.143+72T=
ENST00000274507.5:c.143+72T= ENSP00000274507.1:n.143+72T=
ENST00000471827.1:n.246+72T=
ENST00000512872.1:c.-74+72T= ENSP00000427012.1:n.-74+72T=
ENST00000514447.2:c.143+72T= ENSP00000421123.2:n.143+72T=
ENST00000522943.5:c.143+72T= ENSP00000429618.1:n.143+72T=
NM_002302.2:c.143+72T= NP_002293.2:n.143+72T=
NM_002302.3:c.143+72T= MANE Select NP_002293.2:n.143+72T=