Canonical Allele Identifier: CA1095688

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151811416T>C , CM000663.2:g.151811416T>C	GRCh38
NC_000001.10:g.151783892T>C , CM000663.1:g.151783892T>C	GRCh37
NC_000001.9:g.150050516T>C	NCBI36
NG_029118.1:g.25457A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005060.4:c.1304A>G MANE Select	NP_005051.2:p.Glu435Gly
ENST00000318247.7:c.1304A>G MANE Select	ENSP00000327025.6:p.Glu435Gly
NM_001001523.1:c.1241A>G	NP_001001523.1:p.Glu414Gly
NM_001001523.2:c.1241A>G	NP_001001523.1:p.Glu414Gly
NM_005060.3:c.1304A>G	NP_005051.2:p.Glu435Gly
ENST00000318247.6:c.1304A>G	ENSP00000327025.6:p.Glu435Gly
ENST00000356728.10:c.1241A>G	ENSP00000349164.6:p.Glu414Gly
ENST00000356728.11:c.1241A>G	ENSP00000349164.6:p.Glu414Gly
ENST00000480719.1:n.3374A>G
ENST00000638901.1:c.1495A>G
ENST00000651814.1:c.*261A>G	ENSP00000498691.1:n.*261A>G
ENST00000651893.1:c.581A>G
ENST00000652040.2:c.1019A>G	ENSP00000498548.2:p.Glu340Gly
ENST00000697811.1:c.952A>G	ENSP00000513447.1:p.Arg318Gly
XM_006711484.2:c.1703A>G	XP_006711547.2:p.Glu568Gly
XM_006711484.4:c.1703A>G	XP_006711547.2:p.Glu568Gly
XR_426792.2:n.2065A>G