Canonical Allele Identifier: CA446550881

Gene: LECT2

Linked Data

• MyVariant Identifiers: chr5:g.135288646C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135952957C>A , CM000667.2:g.135952957C>A	GRCh38
NC_000005.9:g.135288646C>A , CM000667.1:g.135288646C>A	GRCh37
NC_000005.8:g.135316545C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274507.6:c.57G>T MANE Select	ENSP00000274507.1:p.Gly19=
ENST00000274507.5:c.57G>T	ENSP00000274507.1:p.Gly19=
ENST00000471827.1:n.160G>T
ENST00000512872.1:c.-160G>T	ENSP00000427012.1:n.-160G>T
ENST00000514447.2:c.57G>T	ENSP00000421123.2:p.Gly19=
ENST00000522943.5:c.57G>T	ENSP00000429618.1:p.Gly19=
NM_002302.2:c.57G>T	NP_002293.2:p.Gly19=
NM_002302.3:c.57G>T MANE Select	NP_002293.2:p.Gly19=