Canonical Allele Identifier: CA272121278
Gene: RORA HGNC NCBI
RORA-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60608764C>T , CM000677.2:g.60608764C>T GRCh38
NC_000015.9:g.60900963C>T , CM000677.1:g.60900963C>T GRCh37
NC_000015.8:g.58688255C>T NCBI36
NG_029246.1:g.625540G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.196+69893G>A (RORA) MANE Select ENSP00000335087.6:n.196+69893G>A
ENST00000261523.9:c.137+18474G>A (RORA) ENSP00000261523.5:n.137+18474G>A
ENST00000309157.8:c.271+6130G>A (RORA) ENSP00000309753.3:n.271+6130G>A
ENST00000335670.10:c.196+69893G>A (RORA) ENSP00000335087.6:n.196+69893G>A
ENST00000551975.5:c.193+68387G>A (RORA)
ENST00000557822.5:n.221+69893G>A (RORA)
ENST00000560004.5:n.151+69893G>A (RORA)
NM_002943.3:c.271+6130G>A (RORA) NP_002934.1:n.271+6130G>A
NM_134260.2:c.137+18474G>A (RORA) NP_599022.1:n.137+18474G>A
NM_134261.2:c.196+69893G>A (RORA) NP_599023.1:n.196+69893G>A
NR_120341.1:n.499+7707C>T (RORA-AS1)
NR_120342.1:n.567+7707C>T (RORA-AS1)
XM_005254584.3:c.58+69893G>A (RORA) XP_005254641.1:n.58+69893G>A
XM_011521875.1:c.139+69893G>A (RORA) XP_011520177.1:n.139+69893G>A
XM_011521876.1:c.64+69893G>A (RORA) XP_011520178.1:n.64+69893G>A
XM_011521878.1:c.-216+68387G>A (RORA) XP_011520180.1:n.-216+68387G>A
XM_005254584.5:c.58+69893G>A (RORA) XP_005254641.1:n.58+69893G>A
XM_011521875.2:c.139+69893G>A (RORA) XP_011520177.1:n.139+69893G>A
XM_011521878.2:c.-216+68387G>A (RORA) XP_011520180.1:n.-216+68387G>A
XM_017022467.2:c.-216+18474G>A (RORA) XP_016877956.1:n.-216+18474G>A
NM_134261.3:c.196+69893G>A (RORA) MANE Select NP_599023.1:n.196+69893G>A
NM_002943.4:c.271+6130G>A (RORA) NP_002934.1:n.271+6130G>A
NM_134260.3:c.137+18474G>A (RORA) NP_599022.1:n.137+18474G>A
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