Canonical Allele Identifier: CA361050783

Gene: LECT2

Linked Data

• gnomAD v4: 5-135952956-G-A
• MyVariant Identifiers: chr5:g.135288645G>A (hg19) ; chr5:g.135952956G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000274507.6:c.58C>T MANE Select	ENSP00000274507.1:p.Pro20Ser
ENST00000274507.5:c.58C>T	ENSP00000274507.1:p.Pro20Ser
ENST00000471827.1:n.161C>T
ENST00000512872.1:c.-159C>T	ENSP00000427012.1:n.-159C>T
ENST00000514447.2:c.58C>T	ENSP00000421123.2:p.Pro20Ser
ENST00000522943.5:c.58C>T	ENSP00000429618.1:p.Pro20Ser
NM_002302.2:c.58C>T	NP_002293.2:p.Pro20Ser
NM_002302.3:c.58C>T MANE Select	NP_002293.2:p.Pro20Ser