Canonical Allele Identifier: CA420913042

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151813492T>C , CM000663.2:g.151813492T>C	GRCh38
NC_000001.10:g.151785968T>C , CM000663.1:g.151785968T>C	GRCh37
NC_000001.9:g.150052592T>C	NCBI36
NG_029118.1:g.23381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.777A>G	ENSP00000498548.2:p.Lys259=
ENST00000697811.1:c.933+1082A>G	ENSP00000513447.1:n.933+1082A>G
ENST00000697812.1:n.200A>G
ENST00000697813.1:n.1057A>G
ENST00000318247.7:c.1062A>G MANE Select	ENSP00000327025.6:p.Lys354=
ENST00000356728.11:c.999A>G	ENSP00000349164.6:p.Lys333=
ENST00000638901.1:c.1253A>G
ENST00000651814.1:c.*19A>G	ENSP00000498691.1:n.*19A>G
ENST00000651893.1:c.344-146A>G
ENST00000318247.6:c.1062A>G	ENSP00000327025.6:p.Lys354=
ENST00000356728.10:c.999A>G	ENSP00000349164.6:p.Lys333=
ENST00000480719.1:n.1298A>G
NM_001001523.1:c.999A>G	NP_001001523.1:p.Lys333=
NM_005060.3:c.1062A>G	NP_005051.2:p.Lys354=
XM_006711484.2:c.1461A>G	XP_006711547.2:p.Lys487=
XR_426792.2:n.1823A>G
XM_006711484.4:c.1461A>G	XP_006711547.2:p.Lys487=
NM_005060.4:c.1062A>G MANE Select	NP_005051.2:p.Lys354=
NM_001001523.2:c.999A>G	NP_001001523.1:p.Lys333=