Canonical Allele Identifier: CA420772345

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151807484C>A , CM000663.2:g.151807484C>A	GRCh38
NC_000001.10:g.151779960C>A , CM000663.1:g.151779960C>A	GRCh37
NC_000001.9:g.150046584C>A	NCBI36
NG_029118.1:g.29389G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.1260G>T	ENSP00000498548.2:p.Gly420=
ENST00000697811.1:c.*227G>T	ENSP00000513447.1:n.*227G>T
ENST00000318247.7:c.1545G>T MANE Select	ENSP00000327025.6:p.Gly515=
ENST00000356728.11:c.1482G>T	ENSP00000349164.6:p.Gly494=
ENST00000638901.1:c.1736G>T
ENST00000651814.1:c.*502G>T	ENSP00000498691.1:n.*502G>T
ENST00000651893.1:c.822G>T
ENST00000318247.6:c.1545G>T	ENSP00000327025.6:p.Gly515=
ENST00000356728.10:c.1482G>T	ENSP00000349164.6:p.Gly494=
ENST00000480719.1:n.3615G>T
NM_001001523.1:c.1482G>T	NP_001001523.1:p.Gly494=
NM_005060.3:c.1545G>T	NP_005051.2:p.Gly515=
XM_006711484.2:c.1944G>T	XP_006711547.2:p.Gly648=
XM_006711484.4:c.1944G>T	XP_006711547.2:p.Gly648=
NM_005060.4:c.1545G>T MANE Select	NP_005051.2:p.Gly515=
NM_001001523.2:c.1482G>T	NP_001001523.1:p.Gly494=