Canonical Allele Identifier: CA1584763444
Gene: LECT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952855T= , CM000667.2:g.135952855T= GRCh38
NC_000005.9:g.135288544T= , CM000667.1:g.135288544T= GRCh37
NC_000005.8:g.135316443T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.143+16A= MANE Select ENSP00000274507.1:n.143+16A=
ENST00000274507.5:c.143+16A= ENSP00000274507.1:n.143+16A=
ENST00000471827.1:n.246+16A=
ENST00000512872.1:c.-74+16A= ENSP00000427012.1:n.-74+16A=
ENST00000514447.2:c.143+16A= ENSP00000421123.2:n.143+16A=
ENST00000522943.5:c.143+16A= ENSP00000429618.1:n.143+16A=
NM_002302.2:c.143+16A= NP_002293.2:n.143+16A=
NM_002302.3:c.143+16A= MANE Select NP_002293.2:n.143+16A=
Search 100 bp 5'
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