Canonical Allele Identifier: CA1506854262

Gene: RXFP1

Linked Data

• dbSNP Id: rs1671852076

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645145_158645154del , CM000666.2:g.158645145_158645154del	GRCh38
NC_000004.11:g.159566297_159566306del , CM000666.1:g.159566297_159566306del	GRCh37
NC_000004.10:g.159785747_159785756del	NCBI36
NG_031835.1:g.128432_128441del
NG_031835.2:g.128432_128441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+7_1345+16del MANE Select	ENSP00000303248.5:n.1345+7_1345+16del
ENST00000307765.9:c.1345+7_1345+16del	ENSP00000303248.5:n.1345+7_1345+16del
ENST00000342048.9:c.*955+7_*955+16del	ENSP00000432036.1:n.*955+7_*955+16del
ENST00000343542.9:c.1201+7_1201+16del	ENSP00000345889.5:n.1201+7_1201+16del
ENST00000423548.5:c.1426+7_1426+16del	ENSP00000405841.2:n.1426+7_1426+16del
ENST00000448688.6:c.877+7_877+16del	ENSP00000414885.3:n.877+7_877+16del
ENST00000460056.6:c.1102+7_1102+16del	ENSP00000423306.1:n.1102+7_1102+16del
ENST00000470033.2:c.1246+7_1246+16del	ENSP00000420712.1:n.1246+7_1246+16del
ENST00000471616.5:c.1398+7_1398+16del	ENSP00000434475.1:n.1398+7_1398+16del
ENST00000613319.4:c.952+7_952+16del	ENSP00000480522.1:n.952+7_952+16del
NM_001253727.1:c.1426+7_1426+16del	NP_001240656.1:n.1426+7_1426+16del
NM_001253728.1:c.1246+7_1246+16del	NP_001240657.1:n.1246+7_1246+16del
NM_001253729.1:c.1201+7_1201+16del	NP_001240658.1:n.1201+7_1201+16del
NM_001253730.1:c.952+7_952+16del	NP_001240659.1:n.952+7_952+16del
NM_001253732.1:c.949+7_949+16del	NP_001240661.1:n.949+7_949+16del
NM_001253733.1:c.877+7_877+16del	NP_001240662.1:n.877+7_877+16del
NM_021634.3:c.1345+7_1345+16del	NP_067647.2:n.1345+7_1345+16del
NR_045579.1:n.2225+7_2225+16del
NR_045580.1:n.1661+7_1661+16del
NR_045581.1:n.1632+7_1632+16del
NR_045582.1:n.1569+7_1569+16del
NR_045583.1:n.1548+7_1548+16del
NR_045584.1:n.1661+7_1661+16del
XM_011532174.1:c.1423+7_1423+16del	XP_011530476.1:n.1423+7_1423+16del
XM_011532175.1:c.1354+7_1354+16del	XP_011530477.1:n.1354+7_1354+16del
XM_011532176.1:c.1273+7_1273+16del	XP_011530478.1:n.1273+7_1273+16del
XM_011532177.1:c.1183+7_1183+16del	XP_011530479.1:n.1183+7_1183+16del
XM_011532178.1:c.1183+7_1183+16del	XP_011530480.1:n.1183+7_1183+16del
XM_011532179.1:c.1196+5814_1196+5823del	XP_011530481.1:n.1196+5814_1196+5823del
NM_001363776.1:c.1102+7_1102+16del	NP_001350705.1:n.1102+7_1102+16del
XM_011532176.2:c.1273+7_1273+16del	XP_011530478.1:n.1273+7_1273+16del
XM_011532179.2:c.1196+5814_1196+5823del	XP_011530481.1:n.1196+5814_1196+5823del
XM_017008517.1:c.1351+7_1351+16del	XP_016864006.1:n.1351+7_1351+16del
XM_017008518.2:c.1342+7_1342+16del	XP_016864007.1:n.1342+7_1342+16del
XM_017008519.1:c.1183+7_1183+16del	XP_016864008.1:n.1183+7_1183+16del
XM_017008520.1:c.1183+7_1183+16del	XP_016864009.1:n.1183+7_1183+16del
XM_017008522.1:c.1099+7_1099+16del	XP_016864011.1:n.1099+7_1099+16del
XM_017008523.2:c.1115+5814_1115+5823del	XP_016864012.1:n.1115+5814_1115+5823del
XM_017008524.2:c.1043+5814_1043+5823del	XP_016864013.1:n.1043+5814_1043+5823del
XM_017008525.1:c.1016+5814_1016+5823del	XP_016864014.1:n.1016+5814_1016+5823del
XM_017008526.1:c.877+7_877+16del	XP_016864015.1:n.877+7_877+16del
NM_021634.4:c.1345+7_1345+16del MANE Select	NP_067647.2:n.1345+7_1345+16del
NM_001253728.2:c.1246+7_1246+16del	NP_001240657.1:n.1246+7_1246+16del
NM_001253729.2:c.1201+7_1201+16del	NP_001240658.1:n.1201+7_1201+16del
NM_001253732.2:c.949+7_949+16del	NP_001240661.1:n.949+7_949+16del
NR_045579.2:n.2057+7_2057+16del
NR_045580.2:n.1493+7_1493+16del
NR_045581.2:n.1464+7_1464+16del
NR_045582.2:n.1401+7_1401+16del
NR_045583.2:n.1380+7_1380+16del
NR_045584.2:n.1493+7_1493+16del
NM_001253727.2:c.1426+7_1426+16del	NP_001240656.1:n.1426+7_1426+16del
NM_001253730.2:c.952+7_952+16del	NP_001240659.1:n.952+7_952+16del
NM_001253733.2:c.877+7_877+16del	NP_001240662.1:n.877+7_877+16del