Canonical Allele Identifier: CA2675392310
Gene: LECT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952792G>T , CM000667.2:g.135952792G>T GRCh38
NC_000005.9:g.135288481G>T , CM000667.1:g.135288481G>T GRCh37
NC_000005.8:g.135316380G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.143+79C>A MANE Select ENSP00000274507.1:n.143+79C>A
ENST00000274507.5:c.143+79C>A ENSP00000274507.1:n.143+79C>A
ENST00000471827.1:n.246+79C>A
ENST00000512872.1:c.-74+79C>A ENSP00000427012.1:n.-74+79C>A
ENST00000514447.2:c.143+79C>A ENSP00000421123.2:n.143+79C>A
ENST00000522943.5:c.143+79C>A ENSP00000429618.1:n.143+79C>A
NM_002302.2:c.143+79C>A NP_002293.2:n.143+79C>A
NM_002302.3:c.143+79C>A MANE Select NP_002293.2:n.143+79C>A