Canonical Allele Identifier: CA347974577

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029524T>C (hg19) ; chr2:g.101413062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101413062T>C , CM000664.2:g.101413062T>C	GRCh38
NC_000002.11:g.102029524T>C , CM000664.1:g.102029524T>C	GRCh37
NC_000002.10:g.101395956T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.910A>G	ENSP00000494249.2:p.Met304Val
ENST00000428343.6:c.571A>G MANE Select	ENSP00000401536.1:p.Met191Val
ENST00000646446.1:c.784A>G	ENSP00000494216.1:p.Met262Val
ENST00000646893.1:c.697A>G	ENSP00000494249.1:p.Met233Val
ENST00000428343.5:c.571A>G	ENSP00000401536.1:p.Met191Val
ENST00000481179.5:c.*287A>G	ENSP00000422968.1:n.*287A>G
NM_001145664.1:c.571A>G	NP_001139136.1:p.Met191Val
XM_011511771.1:c.799A>G	XP_011510073.1:p.Met267Val
XM_011511772.1:c.784A>G	XP_011510074.1:p.Met262Val
XM_011511773.1:c.481A>G	XP_011510075.1:p.Met161Val
XM_011511774.1:c.799A>G	XP_011510076.1:p.Met267Val
XM_011511775.1:c.799A>G	XP_011510077.1:p.Met267Val
XM_011511776.1:c.283A>G	XP_011510078.1:p.Met95Val
XM_011511777.1:c.283A>G	XP_011510079.1:p.Met95Val
XM_011511778.1:c.283A>G	XP_011510080.1:p.Met95Val
XM_011511779.1:c.740A>G	XP_011510081.1:p.Asn247Ser
XM_011511771.2:c.799A>G	XP_011510073.1:p.Met267Val
XM_011511777.2:c.283A>G	XP_011510079.1:p.Met95Val
XM_017004851.1:c.910A>G	XP_016860340.1:p.Met304Val
XM_017004852.1:c.697A>G	XP_016860341.1:p.Met233Val
XM_017004853.1:c.910A>G	XP_016860342.1:p.Met304Val
XM_017004854.1:c.910A>G	XP_016860343.1:p.Met304Val
XR_001738924.1:n.854A>G
NM_001145664.2:c.571A>G MANE Select	NP_001139136.2:p.Met191Val
NM_001367508.1:c.58A>G	NP_001354437.1:p.Met20Val
NM_001367509.1:c.58A>G	NP_001354438.1:p.Met20Val
NM_001367510.1:c.58A>G	NP_001354439.1:p.Met20Val