Canonical Allele Identifier: CA342014025

Gene: RORC

Linked Data

• MyVariant Identifiers: chr1:g.151787066G>C (hg19) ; chr1:g.151814590G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151814590G>C , CM000663.2:g.151814590G>C	GRCh38
NC_000001.10:g.151787066G>C , CM000663.1:g.151787066G>C	GRCh37
NC_000001.9:g.150053690G>C	NCBI36
NG_029118.1:g.22283C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.632C>G	ENSP00000498548.2:p.Thr211Ser
ENST00000697811.1:c.917C>G	ENSP00000513447.1:p.Thr306Ser
ENST00000697812.1:n.55C>G
ENST00000697813.1:n.912C>G
ENST00000318247.7:c.917C>G MANE Select	ENSP00000327025.6:p.Thr306Ser
ENST00000356728.11:c.854C>G	ENSP00000349164.6:p.Thr285Ser
ENST00000638901.1:c.1108C>G
ENST00000651814.1:c.917C>G	ENSP00000498691.1:p.Thr306Ser
ENST00000651893.1:c.327C>G
ENST00000318247.6:c.917C>G	ENSP00000327025.6:p.Thr306Ser
ENST00000356728.10:c.854C>G	ENSP00000349164.6:p.Thr285Ser
ENST00000480719.1:n.200C>G
NM_001001523.1:c.854C>G	NP_001001523.1:p.Thr285Ser
NM_005060.3:c.917C>G	NP_005051.2:p.Thr306Ser
XM_006711484.2:c.1316C>G	XP_006711547.2:p.Thr439Ser
XR_426792.2:n.1596C>G
XM_006711484.4:c.1316C>G	XP_006711547.2:p.Thr439Ser
NM_005060.4:c.917C>G MANE Select	NP_005051.2:p.Thr306Ser
NM_001001523.2:c.854C>G	NP_001001523.1:p.Thr285Ser