Canonical Allele Identifier: CA789734749
Gene: RXFP1 HGNC NCBI

Linked Data

dbSNP Id: rs1315133218

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.158645434_158645436dup , CM000666.2:g.158645434_158645436dup GRCh38
NC_000004.11:g.159566586_159566588dup , CM000666.1:g.159566586_159566588dup GRCh37
NC_000004.10:g.159786036_159786038dup NCBI36
NG_031835.1:g.128721_128723dup
NG_031835.2:g.128721_128723dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307765.10:c.1345+296_1345+298dup MANE Select ENSP00000303248.5:n.1345+296_1345+298dup
ENST00000307765.9:c.1345+296_1345+298dup ENSP00000303248.5:n.1345+296_1345+298dup
ENST00000342048.9:c.*955+296_*955+298dup ENSP00000432036.1:n.*955+296_*955+298dup
ENST00000343542.9:c.1201+296_1201+298dup ENSP00000345889.5:n.1201+296_1201+298dup
ENST00000423548.5:c.1426+296_1426+298dup ENSP00000405841.2:n.1426+296_1426+298dup
ENST00000448688.6:c.877+296_877+298dup ENSP00000414885.3:n.877+296_877+298dup
ENST00000460056.6:c.1102+296_1102+298dup ENSP00000423306.1:n.1102+296_1102+298dup
ENST00000470033.2:c.1246+296_1246+298dup ENSP00000420712.1:n.1246+296_1246+298dup
ENST00000471616.5:c.1398+296_1398+298dup ENSP00000434475.1:n.1398+296_1398+298dup
ENST00000613319.4:c.952+296_952+298dup ENSP00000480522.1:n.952+296_952+298dup
NM_001253727.1:c.1426+296_1426+298dup NP_001240656.1:n.1426+296_1426+298dup
NM_001253728.1:c.1246+296_1246+298dup NP_001240657.1:n.1246+296_1246+298dup
NM_001253729.1:c.1201+296_1201+298dup NP_001240658.1:n.1201+296_1201+298dup
NM_001253730.1:c.952+296_952+298dup NP_001240659.1:n.952+296_952+298dup
NM_001253732.1:c.949+296_949+298dup NP_001240661.1:n.949+296_949+298dup
NM_001253733.1:c.877+296_877+298dup NP_001240662.1:n.877+296_877+298dup
NM_021634.3:c.1345+296_1345+298dup NP_067647.2:n.1345+296_1345+298dup
NR_045579.1:n.2225+296_2225+298dup
NR_045580.1:n.1661+296_1661+298dup
NR_045581.1:n.1632+296_1632+298dup
NR_045582.1:n.1569+296_1569+298dup
NR_045583.1:n.1548+296_1548+298dup
NR_045584.1:n.1661+296_1661+298dup
XM_011532174.1:c.1423+296_1423+298dup XP_011530476.1:n.1423+296_1423+298dup
XM_011532175.1:c.1354+296_1354+298dup XP_011530477.1:n.1354+296_1354+298dup
XM_011532176.1:c.1273+296_1273+298dup XP_011530478.1:n.1273+296_1273+298dup
XM_011532177.1:c.1183+296_1183+298dup XP_011530479.1:n.1183+296_1183+298dup
XM_011532178.1:c.1183+296_1183+298dup XP_011530480.1:n.1183+296_1183+298dup
XM_011532179.1:c.1196+6103_1196+6105dup XP_011530481.1:n.1196+6103_1196+6105dup
NM_001363776.1:c.1102+296_1102+298dup NP_001350705.1:n.1102+296_1102+298dup
XM_011532176.2:c.1273+296_1273+298dup XP_011530478.1:n.1273+296_1273+298dup
XM_011532179.2:c.1196+6103_1196+6105dup XP_011530481.1:n.1196+6103_1196+6105dup
XM_017008517.1:c.1351+296_1351+298dup XP_016864006.1:n.1351+296_1351+298dup
XM_017008518.2:c.1342+296_1342+298dup XP_016864007.1:n.1342+296_1342+298dup
XM_017008519.1:c.1183+296_1183+298dup XP_016864008.1:n.1183+296_1183+298dup
XM_017008520.1:c.1183+296_1183+298dup XP_016864009.1:n.1183+296_1183+298dup
XM_017008522.1:c.1099+296_1099+298dup XP_016864011.1:n.1099+296_1099+298dup
XM_017008523.2:c.1115+6103_1115+6105dup XP_016864012.1:n.1115+6103_1115+6105dup
XM_017008524.2:c.1043+6103_1043+6105dup XP_016864013.1:n.1043+6103_1043+6105dup
XM_017008525.1:c.1016+6103_1016+6105dup XP_016864014.1:n.1016+6103_1016+6105dup
XM_017008526.1:c.877+296_877+298dup XP_016864015.1:n.877+296_877+298dup
NM_021634.4:c.1345+296_1345+298dup MANE Select NP_067647.2:n.1345+296_1345+298dup
NM_001253728.2:c.1246+296_1246+298dup NP_001240657.1:n.1246+296_1246+298dup
NM_001253729.2:c.1201+296_1201+298dup NP_001240658.1:n.1201+296_1201+298dup
NM_001253732.2:c.949+296_949+298dup NP_001240661.1:n.949+296_949+298dup
NR_045579.2:n.2057+296_2057+298dup
NR_045580.2:n.1493+296_1493+298dup
NR_045581.2:n.1464+296_1464+298dup
NR_045582.2:n.1401+296_1401+298dup
NR_045583.2:n.1380+296_1380+298dup
NR_045584.2:n.1493+296_1493+298dup
NM_001253727.2:c.1426+296_1426+298dup NP_001240656.1:n.1426+296_1426+298dup
NM_001253730.2:c.952+296_952+298dup NP_001240659.1:n.952+296_952+298dup
NM_001253733.2:c.877+296_877+298dup NP_001240662.1:n.877+296_877+298dup