Canonical Allele Identifier: CA909516847

Gene: LRIG1

Linked Data

• dbSNP Id: rs11706832
• gnomAD v3: 3-66452557-A-G
• gnomAD v4: 3-66452557-A-G
• MyVariant Identifiers: chr3:g.66502981A>G (hg19) ; chr3:g.66452557A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66452557A>G , CM000665.2:g.66452557A>G	GRCh38
NC_000003.11:g.66502981A>G , CM000665.1:g.66502981A>G	GRCh37
NC_000003.10:g.66585671A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000273261.8:c.291-924T>C MANE Select	ENSP00000273261.3:n.291-924T>C
ENST00000273261.7:c.291-924T>C	ENSP00000273261.3:n.291-924T>C
ENST00000383703.3:c.291-924T>C	ENSP00000373208.3:n.291-924T>C
ENST00000475366.5:n.186-924T>C
ENST00000495671.1:n.334-924T>C
ENST00000498287.5:n.244-924T>C
NM_015541.2:c.291-924T>C	NP_056356.2:n.291-924T>C
XM_011533578.1:c.291-924T>C	XP_011531880.1:n.291-924T>C
XM_011533579.1:c.-490-924T>C	XP_011531881.1:n.-490-924T>C
XM_011533578.2:c.291-924T>C	XP_011531880.1:n.291-924T>C
XM_011533579.3:c.-490-924T>C	XP_011531881.1:n.-490-924T>C
XM_017006134.2:c.290+9881T>C	XP_016861623.1:n.290+9881T>C
XM_017006136.2:c.-490-924T>C	XP_016861625.1:n.-490-924T>C
NM_001377344.1:c.290+9881T>C	NP_001364273.1:n.290+9881T>C
NM_001377345.1:c.-490-924T>C	NP_001364274.1:n.-490-924T>C
NM_001377346.1:c.-490-924T>C	NP_001364275.1:n.-490-924T>C
NM_015541.3:c.291-924T>C MANE Select	NP_056356.2:n.291-924T>C