Canonical Allele Identifier: CA2573131016

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151807641T>C , CM000663.2:g.151807641T>C	GRCh38
NC_000001.10:g.151780117T>C , CM000663.1:g.151780117T>C	GRCh37
NC_000001.9:g.150046741T>C	NCBI36
NG_029118.1:g.29232A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.1111-8A>G	ENSP00000498548.2:n.1111-8A>G
ENST00000697811.1:c.*78-8A>G	ENSP00000513447.1:n.*78-8A>G
ENST00000318247.7:c.1396-8A>G MANE Select	ENSP00000327025.6:n.1396-8A>G
ENST00000356728.11:c.1333-8A>G	ENSP00000349164.6:n.1333-8A>G
ENST00000638901.1:c.1587-8A>G
ENST00000651814.1:c.*353-8A>G	ENSP00000498691.1:n.*353-8A>G
ENST00000651893.1:c.673-8A>G
ENST00000318247.6:c.1396-8A>G	ENSP00000327025.6:n.1396-8A>G
ENST00000356728.10:c.1333-8A>G	ENSP00000349164.6:n.1333-8A>G
ENST00000480719.1:n.3466-8A>G
NM_001001523.1:c.1333-8A>G	NP_001001523.1:n.1333-8A>G
NM_005060.3:c.1396-8A>G	NP_005051.2:n.1396-8A>G
XM_006711484.2:c.1795-8A>G	XP_006711547.2:n.1795-8A>G
XR_426792.2:n.2157-8A>G
XM_006711484.4:c.1795-8A>G	XP_006711547.2:n.1795-8A>G
NM_005060.4:c.1396-8A>G MANE Select	NP_005051.2:n.1396-8A>G
NM_001001523.2:c.1333-8A>G	NP_001001523.1:n.1333-8A>G