Canonical Allele Identifier: CA1371691639

Gene: LRIG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66410028C= , CM000665.2:g.66410028C=	GRCh38
NC_000003.11:g.66460452C= , CM000665.1:g.66460452C=	GRCh37
NC_000003.10:g.66543142C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015541.3:c.935+101G= MANE Select	NP_056356.2:n.935+101G=
ENST00000273261.8:c.935+101G= MANE Select	ENSP00000273261.3:n.935+101G=
NM_001377344.1:c.860+101G=	NP_001364273.1:n.860+101G=
NM_001377345.1:c.155+101G=	NP_001364274.1:n.155+101G=
NM_001377346.1:c.155+101G=	NP_001364275.1:n.155+101G=
NM_015541.2:c.935+101G=	NP_056356.2:n.935+101G=
ENST00000273261.7:c.935+101G=	ENSP00000273261.3:n.935+101G=
ENST00000383703.3:c.935+101G=	ENSP00000373208.3:n.935+101G=
ENST00000491821.1:n.306G=
XM_011533578.1:c.792-2537G=	XP_011531880.1:n.792-2537G=
XM_011533578.2:c.792-2537G=	XP_011531880.1:n.792-2537G=
XM_011533579.1:c.155+101G=	XP_011531881.1:n.155+101G=
XM_011533579.3:c.155+101G=	XP_011531881.1:n.155+101G=
XM_017006134.2:c.860+101G=	XP_016861623.1:n.860+101G=
XM_017006135.1:c.257+101G=	XP_016861624.1:n.257+101G=
XM_017006136.2:c.155+101G=	XP_016861625.1:n.155+101G=