Canonical Allele Identifier: CA1506854245

Gene: RXFP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645095_158645096delinsGT , CM000666.2:g.158645095_158645096delinsGT	GRCh38
NC_000004.11:g.159566247_159566248delinsGT , CM000666.1:g.159566247_159566248delinsGT	GRCh37
NC_000004.10:g.159785697_159785698delinsGT	NCBI36
NG_031835.1:g.128382_128383delinsGT
NG_031835.2:g.128382_128383delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1302_1303delinsGT MANE Select	ENSP00000303248.5:p.Arg434=
ENST00000307765.9:c.1302_1303delinsGT	ENSP00000303248.5:p.Arg434=
ENST00000342048.9:c.*912_*913delinsGT	ENSP00000432036.1:n.*912_*913delinsGT
ENST00000343542.9:c.1158_1159delinsGT	ENSP00000345889.5:p.Arg386=
ENST00000423548.5:c.1383_1384delinsGT	ENSP00000405841.2:p.Arg461=
ENST00000448688.6:c.834_835delinsGT	ENSP00000414885.3:p.Arg278=
ENST00000460056.6:c.1059_1060delinsGT	ENSP00000423306.1:p.Arg353=
ENST00000470033.2:c.1203_1204delinsGT	ENSP00000420712.1:p.Arg401=
ENST00000471616.5:c.1355_1356delinsGT	ENSP00000434475.1:n.1355_1356delinsGT
ENST00000613319.4:c.909_910delinsGT	ENSP00000480522.1:p.Arg303=
NM_001253727.1:c.1383_1384delinsGT	NP_001240656.1:p.Arg461=
NM_001253728.1:c.1203_1204delinsGT	NP_001240657.1:p.Arg401=
NM_001253729.1:c.1158_1159delinsGT	NP_001240658.1:p.Arg386=
NM_001253730.1:c.909_910delinsGT	NP_001240659.1:p.Arg303=
NM_001253732.1:c.906_907delinsGT	NP_001240661.1:p.Arg302=
NM_001253733.1:c.834_835delinsGT	NP_001240662.1:p.Arg278=
NM_021634.3:c.1302_1303delinsGT	NP_067647.2:p.Arg434=
NR_045579.1:n.2182_2183delinsGT
NR_045580.1:n.1618_1619delinsGT
NR_045581.1:n.1589_1590delinsGT
NR_045582.1:n.1526_1527delinsGT
NR_045583.1:n.1505_1506delinsGT
NR_045584.1:n.1618_1619delinsGT
XM_011532174.1:c.1380_1381delinsGT	XP_011530476.1:p.Arg460=
XM_011532175.1:c.1311_1312delinsGT	XP_011530477.1:p.Arg437=
XM_011532176.1:c.1230_1231delinsGT	XP_011530478.1:p.Arg410=
XM_011532177.1:c.1140_1141delinsGT	XP_011530479.1:p.Arg380=
XM_011532178.1:c.1140_1141delinsGT	XP_011530480.1:p.Arg380=
XM_011532179.1:c.1196+5764_1196+5765delinsGT	XP_011530481.1:n.1196+5764_1196+5765delinsGT
NM_001363776.1:c.1059_1060delinsGT	NP_001350705.1:p.Arg353=
XM_011532176.2:c.1230_1231delinsGT	XP_011530478.1:p.Arg410=
XM_011532179.2:c.1196+5764_1196+5765delinsGT	XP_011530481.1:n.1196+5764_1196+5765delinsGT
XM_017008517.1:c.1308_1309delinsGT	XP_016864006.1:p.Arg436=
XM_017008518.2:c.1299_1300delinsGT	XP_016864007.1:p.Arg433=
XM_017008519.1:c.1140_1141delinsGT	XP_016864008.1:p.Arg380=
XM_017008520.1:c.1140_1141delinsGT	XP_016864009.1:p.Arg380=
XM_017008522.1:c.1056_1057delinsGT	XP_016864011.1:p.Arg352=
XM_017008523.2:c.1115+5764_1115+5765delinsGT	XP_016864012.1:n.1115+5764_1115+5765delinsGT
XM_017008524.2:c.1043+5764_1043+5765delinsGT	XP_016864013.1:n.1043+5764_1043+5765delinsGT
XM_017008525.1:c.1016+5764_1016+5765delinsGT	XP_016864014.1:n.1016+5764_1016+5765delinsGT
XM_017008526.1:c.834_835delinsGT	XP_016864015.1:p.Arg278=
NM_021634.4:c.1302_1303delinsGT MANE Select	NP_067647.2:p.Arg434=
NM_001253728.2:c.1203_1204delinsGT	NP_001240657.1:p.Arg401=
NM_001253729.2:c.1158_1159delinsGT	NP_001240658.1:p.Arg386=
NM_001253732.2:c.906_907delinsGT	NP_001240661.1:p.Arg302=
NR_045579.2:n.2014_2015delinsGT
NR_045580.2:n.1450_1451delinsGT
NR_045581.2:n.1421_1422delinsGT
NR_045582.2:n.1358_1359delinsGT
NR_045583.2:n.1337_1338delinsGT
NR_045584.2:n.1450_1451delinsGT
NM_001253727.2:c.1383_1384delinsGT	NP_001240656.1:p.Arg461=
NM_001253730.2:c.909_910delinsGT	NP_001240659.1:p.Arg303=
NM_001253733.2:c.834_835delinsGT	NP_001240662.1:p.Arg278=