Canonical Allele Identifier: CA361050785
Gene: LECT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135288645G>T (hg19) chr5:g.135952956G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952956G>T , CM000667.2:g.135952956G>T GRCh38
NC_000005.9:g.135288645G>T , CM000667.1:g.135288645G>T GRCh37
NC_000005.8:g.135316544G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.58C>A MANE Select ENSP00000274507.1:p.Pro20Thr
ENST00000274507.5:c.58C>A ENSP00000274507.1:p.Pro20Thr
ENST00000471827.1:n.161C>A
ENST00000512872.1:c.-159C>A ENSP00000427012.1:n.-159C>A
ENST00000514447.2:c.58C>A ENSP00000421123.2:p.Pro20Thr
ENST00000522943.5:c.58C>A ENSP00000429618.1:p.Pro20Thr
NM_002302.2:c.58C>A NP_002293.2:p.Pro20Thr
NM_002302.3:c.58C>A MANE Select NP_002293.2:p.Pro20Thr
Search 100 bp 5'
Search 100 bp 3'