Canonical Allele Identifier: CA132438470
Gene: RANBP17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.171293729C>G , CM000667.2:g.171293729C>G GRCh38
NC_000005.9:g.170720733C>G , CM000667.1:g.170720733C>G GRCh37
NC_000005.8:g.170653338C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523189.6:c.2944-154C>G MANE Select ENSP00000427975.1:n.2944-154C>G
ENST00000389118.8:c.*1497-154C>G ENSP00000373770.4:n.*1497-154C>G
ENST00000519949.5:c.*1391-154C>G ENSP00000430444.1:n.*1391-154C>G
ENST00000521759.5:n.1291-154C>G
ENST00000522066.5:c.*1500-154C>G ENSP00000430958.1:n.*1500-154C>G
ENST00000522533.5:c.*1331-154C>G ENSP00000430599.1:n.*1331-154C>G
ENST00000523189.5:c.2944-154C>G ENSP00000427975.1:n.2944-154C>G
ENST00000616486.1:c.1234-154C>G ENSP00000478243.1:n.1234-154C>G
NM_022897.4:c.2944-154C>G NP_075048.1:n.2944-154C>G
XM_011534625.1:c.3016-154C>G XP_011532927.1:n.3016-154C>G
XM_011534626.1:c.3004-154C>G XP_011532928.1:n.3004-154C>G
XM_011534627.1:c.2956-154C>G XP_011532929.1:n.2956-154C>G
XM_011534628.1:c.2896-154C>G XP_011532930.1:n.2896-154C>G
XM_011534629.1:c.3022-154C>G XP_011532931.1:n.3022-154C>G
XM_011534630.1:c.2869-154C>G XP_011532932.1:n.2869-154C>G
XM_011534631.1:c.2950-154C>G XP_011532933.1:n.2950-154C>G
XM_011534633.1:c.2770-154C>G XP_011532935.1:n.2770-154C>G
XM_011534634.1:c.2569-154C>G XP_011532936.1:n.2569-154C>G
XM_011534635.1:c.2116-154C>G XP_011532937.1:n.2116-154C>G
XR_941107.1:n.2857-154C>G
XM_017009736.1:c.2836-154C>G XP_016865225.1:n.2836-154C>G
XM_017009738.1:c.2809-154C>G XP_016865227.1:n.2809-154C>G
XM_017009739.1:c.2797-154C>G XP_016865228.1:n.2797-154C>G
XM_017009740.1:c.2677-154C>G XP_016865229.1:n.2677-154C>G
XM_017009743.1:c.2710-154C>G XP_016865232.1:n.2710-154C>G
XM_017009745.1:c.2056-154C>G XP_016865234.1:n.2056-154C>G
XM_017009747.1:c.1327-154C>G XP_016865236.1:n.1327-154C>G
XR_001742202.1:n.2797-154C>G
NM_022897.5:c.2944-154C>G MANE Select NP_075048.1:n.2944-154C>G
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