Canonical Allele Identifier: CA76535648
Gene: LRIG1 HGNC NCBI

Linked Data

dbSNP Id: rs13078828
gnomAD v2: 3-66479487-G-A
gnomAD v3: 3-66429063-G-A
gnomAD v4: 3-66429063-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.66429063G>A , CM000665.2:g.66429063G>A GRCh38
NC_000003.11:g.66479487G>A , CM000665.1:g.66479487G>A GRCh37
NC_000003.10:g.66562177G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273261.8:c.366-11797C>T MANE Select ENSP00000273261.3:n.366-11797C>T
ENST00000273261.7:c.366-11797C>T ENSP00000273261.3:n.366-11797C>T
ENST00000383703.3:c.366-11797C>T ENSP00000373208.3:n.366-11797C>T
ENST00000475366.5:n.261-11797C>T
ENST00000498287.5:n.319-11797C>T
NM_015541.2:c.366-11797C>T NP_056356.2:n.366-11797C>T
XM_011533578.1:c.366-11797C>T XP_011531880.1:n.366-11797C>T
XM_011533579.1:c.-415-11797C>T XP_011531881.1:n.-415-11797C>T
XM_011533578.2:c.366-11797C>T XP_011531880.1:n.366-11797C>T
XM_011533579.3:c.-415-11797C>T XP_011531881.1:n.-415-11797C>T
XM_017006134.2:c.291-11797C>T XP_016861623.1:n.291-11797C>T
XM_017006136.2:c.-415-11797C>T XP_016861625.1:n.-415-11797C>T
NM_001377344.1:c.291-11797C>T NP_001364273.1:n.291-11797C>T
NM_001377345.1:c.-415-11797C>T NP_001364274.1:n.-415-11797C>T
NM_001377346.1:c.-415-11797C>T NP_001364275.1:n.-415-11797C>T
NM_015541.3:c.366-11797C>T MANE Select NP_056356.2:n.366-11797C>T