Canonical Allele Identifier: CA2830535175

Gene: RXFP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645282_158645285del , CM000666.2:g.158645282_158645285del	GRCh38
NC_000004.11:g.159566434_159566437del , CM000666.1:g.159566434_159566437del	GRCh37
NC_000004.10:g.159785884_159785887del	NCBI36
NG_031835.1:g.128569_128572del
NG_031835.2:g.128569_128572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+144_1345+147del MANE Select	ENSP00000303248.5:n.1345+144_1345+147del
ENST00000307765.9:c.1345+144_1345+147del	ENSP00000303248.5:n.1345+144_1345+147del
ENST00000342048.9:c.*955+144_*955+147del	ENSP00000432036.1:n.*955+144_*955+147del
ENST00000343542.9:c.1201+144_1201+147del	ENSP00000345889.5:n.1201+144_1201+147del
ENST00000423548.5:c.1426+144_1426+147del	ENSP00000405841.2:n.1426+144_1426+147del
ENST00000448688.6:c.877+144_877+147del	ENSP00000414885.3:n.877+144_877+147del
ENST00000460056.6:c.1102+144_1102+147del	ENSP00000423306.1:n.1102+144_1102+147del
ENST00000470033.2:c.1246+144_1246+147del	ENSP00000420712.1:n.1246+144_1246+147del
ENST00000471616.5:c.1398+144_1398+147del	ENSP00000434475.1:n.1398+144_1398+147del
ENST00000613319.4:c.952+144_952+147del	ENSP00000480522.1:n.952+144_952+147del
NM_001253727.1:c.1426+144_1426+147del	NP_001240656.1:n.1426+144_1426+147del
NM_001253728.1:c.1246+144_1246+147del	NP_001240657.1:n.1246+144_1246+147del
NM_001253729.1:c.1201+144_1201+147del	NP_001240658.1:n.1201+144_1201+147del
NM_001253730.1:c.952+144_952+147del	NP_001240659.1:n.952+144_952+147del
NM_001253732.1:c.949+144_949+147del	NP_001240661.1:n.949+144_949+147del
NM_001253733.1:c.877+144_877+147del	NP_001240662.1:n.877+144_877+147del
NM_021634.3:c.1345+144_1345+147del	NP_067647.2:n.1345+144_1345+147del
NR_045579.1:n.2225+144_2225+147del
NR_045580.1:n.1661+144_1661+147del
NR_045581.1:n.1632+144_1632+147del
NR_045582.1:n.1569+144_1569+147del
NR_045583.1:n.1548+144_1548+147del
NR_045584.1:n.1661+144_1661+147del
XM_011532174.1:c.1423+144_1423+147del	XP_011530476.1:n.1423+144_1423+147del
XM_011532175.1:c.1354+144_1354+147del	XP_011530477.1:n.1354+144_1354+147del
XM_011532176.1:c.1273+144_1273+147del	XP_011530478.1:n.1273+144_1273+147del
XM_011532177.1:c.1183+144_1183+147del	XP_011530479.1:n.1183+144_1183+147del
XM_011532178.1:c.1183+144_1183+147del	XP_011530480.1:n.1183+144_1183+147del
XM_011532179.1:c.1196+5951_1196+5954del	XP_011530481.1:n.1196+5951_1196+5954del
NM_001363776.1:c.1102+144_1102+147del	NP_001350705.1:n.1102+144_1102+147del
XM_011532176.2:c.1273+144_1273+147del	XP_011530478.1:n.1273+144_1273+147del
XM_011532179.2:c.1196+5951_1196+5954del	XP_011530481.1:n.1196+5951_1196+5954del
XM_017008517.1:c.1351+144_1351+147del	XP_016864006.1:n.1351+144_1351+147del
XM_017008518.2:c.1342+144_1342+147del	XP_016864007.1:n.1342+144_1342+147del
XM_017008519.1:c.1183+144_1183+147del	XP_016864008.1:n.1183+144_1183+147del
XM_017008520.1:c.1183+144_1183+147del	XP_016864009.1:n.1183+144_1183+147del
XM_017008522.1:c.1099+144_1099+147del	XP_016864011.1:n.1099+144_1099+147del
XM_017008523.2:c.1115+5951_1115+5954del	XP_016864012.1:n.1115+5951_1115+5954del
XM_017008524.2:c.1043+5951_1043+5954del	XP_016864013.1:n.1043+5951_1043+5954del
XM_017008525.1:c.1016+5951_1016+5954del	XP_016864014.1:n.1016+5951_1016+5954del
XM_017008526.1:c.877+144_877+147del	XP_016864015.1:n.877+144_877+147del
NM_021634.4:c.1345+144_1345+147del MANE Select	NP_067647.2:n.1345+144_1345+147del
NM_001253728.2:c.1246+144_1246+147del	NP_001240657.1:n.1246+144_1246+147del
NM_001253729.2:c.1201+144_1201+147del	NP_001240658.1:n.1201+144_1201+147del
NM_001253732.2:c.949+144_949+147del	NP_001240661.1:n.949+144_949+147del
NR_045579.2:n.2057+144_2057+147del
NR_045580.2:n.1493+144_1493+147del
NR_045581.2:n.1464+144_1464+147del
NR_045582.2:n.1401+144_1401+147del
NR_045583.2:n.1380+144_1380+147del
NR_045584.2:n.1493+144_1493+147del
NM_001253727.2:c.1426+144_1426+147del	NP_001240656.1:n.1426+144_1426+147del
NM_001253730.2:c.952+144_952+147del	NP_001240659.1:n.952+144_952+147del
NM_001253733.2:c.877+144_877+147del	NP_001240662.1:n.877+144_877+147del