Canonical Allele Identifier: CA446550889

Gene: LECT2

Linked Data

• MyVariant Identifiers: chr5:g.135288655T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135952966T>A , CM000667.2:g.135952966T>A	GRCh38
NC_000005.9:g.135288655T>A , CM000667.1:g.135288655T>A	GRCh37
NC_000005.8:g.135316554T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274507.6:c.48A>T MANE Select	ENSP00000274507.1:p.Ala16=
ENST00000274507.5:c.48A>T	ENSP00000274507.1:p.Ala16=
ENST00000471827.1:n.151A>T
ENST00000512872.1:c.-169A>T	ENSP00000427012.1:n.-169A>T
ENST00000514447.2:c.48A>T	ENSP00000421123.2:p.Ala16=
ENST00000522943.5:c.48A>T	ENSP00000429618.1:p.Ala16=
NM_002302.2:c.48A>T	NP_002293.2:p.Ala16=
NM_002302.3:c.48A>T MANE Select	NP_002293.2:p.Ala16=