Canonical Allele Identifier: CA1371723503
Gene: LRIG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.66475539T= , CM000665.2:g.66475539T= GRCh38
NC_000003.11:g.66525963T= , CM000665.1:g.66525963T= GRCh37
NC_000003.10:g.66608653T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015541.3:c.219-13030A= MANE Select NP_056356.2:n.219-13030A=
ENST00000273261.8:c.219-13030A= MANE Select ENSP00000273261.3:n.219-13030A=
NM_001377344.1:c.219-13030A= NP_001364273.1:n.219-13030A=
NM_001377345.1:c.-562-13030A= NP_001364274.1:n.-562-13030A=
NM_001377346.1:c.-562-13030A= NP_001364275.1:n.-562-13030A=
NM_015541.2:c.219-13030A= NP_056356.2:n.219-13030A=
ENST00000273261.7:c.219-13030A= ENSP00000273261.3:n.219-13030A=
ENST00000383703.3:c.219-13030A= ENSP00000373208.3:n.219-13030A=
ENST00000475366.5:n.114-13030A=
ENST00000498287.5:n.172-13030A=
XM_011533578.1:c.219-13030A= XP_011531880.1:n.219-13030A=
XM_011533578.2:c.219-13030A= XP_011531880.1:n.219-13030A=
XM_011533579.1:c.-562-13030A= XP_011531881.1:n.-562-13030A=
XM_011533579.3:c.-562-13030A= XP_011531881.1:n.-562-13030A=
XM_017006134.2:c.219-13030A= XP_016861623.1:n.219-13030A=
XM_017006136.2:c.-562-13030A= XP_016861625.1:n.-562-13030A=