Canonical Allele Identifier: CA11502780
Gene: LRIG1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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