Canonical Allele Identifier: CA24308690

Gene: LRRC7

Linked Data

• dbSNP Id: rs2226284
• MyVariant Identifiers: chr1:g.69869999T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.69869999T>G , CM000663.2:g.69869999T>G	GRCh38
NC_000001.10:g.70335682T>G , CM000663.1:g.70335682T>G	GRCh37
NC_000001.9:g.70108270T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651217.1:n.563+31716T>G
ENST00000651989.2:c.647+31716T>G MANE Select	ENSP00000498937.2:n.647+31716T>G
ENST00000035383.9:c.533+31716T>G	ENSP00000035383.5:n.533+31716T>G
ENST00000310961.9:c.548+31716T>G	ENSP00000309245.4:n.548+31716T>G
ENST00000370958.5:c.648-3468T>G	ENSP00000359997.1:n.648-3468T>G
ENST00000415775.2:c.-873+31716T>G	ENSP00000394867.2:n.-873+31716T>G
NM_020794.2:c.533+31716T>G	NP_065845.1:n.533+31716T>G
XM_011541836.1:c.650+31716T>G	XP_011540138.1:n.650+31716T>G
NM_001330635.1:c.548+31716T>G	NP_001317564.1:n.548+31716T>G
NM_001350216.1:c.650+31716T>G	NP_001337145.1:n.650+31716T>G
NM_001366836.1:c.648-3468T>G	NP_001353765.1:n.648-3468T>G
NM_001366837.1:c.549-3468T>G	NP_001353766.1:n.549-3468T>G
NM_001366838.1:c.647+31716T>G	NP_001353767.1:n.647+31716T>G
NM_001366839.1:c.548+31716T>G	NP_001353768.1:n.548+31716T>G
NM_001366840.1:c.651-3468T>G	NP_001353769.1:n.651-3468T>G
NM_001366841.1:c.548+31716T>G	NP_001353770.1:n.548+31716T>G
NM_001366842.1:c.705-3468T>G	NP_001353771.1:n.705-3468T>G
XM_017001885.1:c.704+31716T>G	XP_016857374.1:n.704+31716T>G
XM_017001886.1:c.704+31716T>G	XP_016857375.1:n.704+31716T>G
XM_017001887.1:c.704+31716T>G	XP_016857376.1:n.704+31716T>G
XM_017001888.1:c.704+31716T>G	XP_016857377.1:n.704+31716T>G
XM_017001889.1:c.704+31716T>G	XP_016857378.1:n.704+31716T>G
XM_017001892.1:c.704+31716T>G	XP_016857381.1:n.704+31716T>G
XM_017001895.1:c.704+31716T>G	XP_016857384.1:n.704+31716T>G
NM_001330635.3:c.548+31716T>G	NP_001317564.1:n.548+31716T>G
NM_001350216.2:c.650+31716T>G	NP_001337145.1:n.650+31716T>G
NM_001366836.3:c.648-3468T>G	NP_001353765.1:n.648-3468T>G
NM_001366837.3:c.549-3468T>G	NP_001353766.1:n.549-3468T>G
NM_001366838.3:c.647+31716T>G	NP_001353767.1:n.647+31716T>G
NM_001366839.3:c.548+31716T>G	NP_001353768.1:n.548+31716T>G
NM_001370785.2:c.647+31716T>G MANE Select	NP_001357714.1:n.647+31716T>G
NM_001350216.3:c.650+31716T>G	NP_001337145.1:n.650+31716T>G