Canonical Allele Identifier: CA2485032

Gene: LRIG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66410216G>A , CM000665.2:g.66410216G>A	GRCh38
NC_000003.11:g.66460640G>A , CM000665.1:g.66460640G>A	GRCh37
NC_000003.10:g.66543330G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273261.8:c.848C>T MANE Select	ENSP00000273261.3:p.Thr283Met
ENST00000273261.7:c.848C>T	ENSP00000273261.3:p.Thr283Met
ENST00000383703.3:c.848C>T	ENSP00000373208.3:p.Thr283Met
ENST00000491821.1:n.118C>T
ENST00000497721.5:n.533C>T
NM_015541.2:c.848C>T	NP_056356.2:p.Thr283Met
XM_011533578.1:c.791+2655C>T	XP_011531880.1:n.791+2655C>T
XM_011533579.1:c.68C>T	XP_011531881.1:p.Thr23Met
XM_011533578.2:c.791+2655C>T	XP_011531880.1:n.791+2655C>T
XM_011533579.3:c.68C>T	XP_011531881.1:p.Thr23Met
XM_017006134.2:c.773C>T	XP_016861623.1:p.Thr258Met
XM_017006135.1:c.170C>T	XP_016861624.1:p.Thr57Met
XM_017006136.2:c.68C>T	XP_016861625.1:p.Thr23Met
NM_001377344.1:c.773C>T	NP_001364273.1:p.Thr258Met
NM_001377345.1:c.68C>T	NP_001364274.1:p.Thr23Met
NM_001377346.1:c.68C>T	NP_001364275.1:p.Thr23Met
NM_015541.3:c.848C>T MANE Select	NP_056356.2:p.Thr283Met