Canonical Allele Identifier: CA1012165

Gene: LRIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113114470A>C , CM000663.2:g.113114470A>C	GRCh38
NC_000001.10:g.113657092A>C , CM000663.1:g.113657092A>C	GRCh37
NC_000001.9:g.113458615A>C	NCBI36
NG_042819.1:g.46301A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014813.3:c.2124A>C MANE Select	NP_055628.1:p.Thr708=
ENST00000361127.6:c.2124A>C MANE Select	ENSP00000355396.4:p.Thr708=
NM_001312686.1:c.1815A>C	NP_001299615.1:p.Thr605=
NM_001312686.2:c.1815A>C	NP_001299615.1:p.Thr605=
NM_014813.2:c.2124A>C	NP_055628.1:p.Thr708=
ENST00000361127.5:c.2124A>C	ENSP00000355396.4:p.Thr708=
ENST00000466161.1:n.1396A>C
ENST00000492207.5:n.903A>C
XM_005271369.1:c.1803A>C	XP_005271426.1:p.Thr601=
XM_005271369.2:c.1803A>C	XP_005271426.1:p.Thr601=
XM_011542497.1:c.1041A>C	XP_011540799.1:p.Thr347=
XM_017002952.2:c.588A>C	XP_016858441.1:p.Thr196=
XM_024451227.1:c.1815A>C	XP_024306995.1:p.Thr605=
XM_024451231.1:c.588A>C	XP_024306999.1:p.Thr196=