Canonical Allele Identifier: CA1095776

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151813552G>A , CM000663.2:g.151813552G>A	GRCh38
NC_000001.10:g.151786028G>A , CM000663.1:g.151786028G>A	GRCh37
NC_000001.9:g.150052652G>A	NCBI36
NG_029118.1:g.23321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.717C>T	ENSP00000498548.2:p.Phe239=
ENST00000697811.1:c.933+1022C>T	ENSP00000513447.1:n.933+1022C>T
ENST00000697812.1:n.140C>T
ENST00000697813.1:n.997C>T
ENST00000318247.7:c.1002C>T MANE Select	ENSP00000327025.6:p.Phe334=
ENST00000356728.11:c.939C>T	ENSP00000349164.6:p.Phe313=
ENST00000638901.1:c.1193C>T
ENST00000651814.1:c.1084C>T	ENSP00000498691.1:p.Arg362Cys
ENST00000651893.1:c.344-206C>T
ENST00000318247.6:c.1002C>T	ENSP00000327025.6:p.Phe334=
ENST00000356728.10:c.939C>T	ENSP00000349164.6:p.Phe313=
ENST00000480719.1:n.1238C>T
NM_001001523.1:c.939C>T	NP_001001523.1:p.Phe313=
NM_005060.3:c.1002C>T	NP_005051.2:p.Phe334=
XM_006711484.2:c.1401C>T	XP_006711547.2:p.Phe467=
XR_426792.2:n.1763C>T
XM_006711484.4:c.1401C>T	XP_006711547.2:p.Phe467=
NM_005060.4:c.1002C>T MANE Select	NP_005051.2:p.Phe334=
NM_001001523.2:c.939C>T	NP_001001523.1:p.Phe313=