Canonical Allele Identifier: CA2672509957

Gene: RXFP1

Linked Data

• gnomAD v4: 4-158645253-TTGCTTGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645258_158645265del , CM000666.2:g.158645258_158645265del	GRCh38
NC_000004.11:g.159566410_159566417del , CM000666.1:g.159566410_159566417del	GRCh37
NC_000004.10:g.159785860_159785867del	NCBI36
NG_031835.1:g.128545_128552del
NG_031835.2:g.128545_128552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+120_1345+127del MANE Select	ENSP00000303248.5:n.1345+120_1345+127del
ENST00000307765.9:c.1345+120_1345+127del	ENSP00000303248.5:n.1345+120_1345+127del
ENST00000342048.9:c.*955+120_*955+127del	ENSP00000432036.1:n.*955+120_*955+127del
ENST00000343542.9:c.1201+120_1201+127del	ENSP00000345889.5:n.1201+120_1201+127del
ENST00000423548.5:c.1426+120_1426+127del	ENSP00000405841.2:n.1426+120_1426+127del
ENST00000448688.6:c.877+120_877+127del	ENSP00000414885.3:n.877+120_877+127del
ENST00000460056.6:c.1102+120_1102+127del	ENSP00000423306.1:n.1102+120_1102+127del
ENST00000470033.2:c.1246+120_1246+127del	ENSP00000420712.1:n.1246+120_1246+127del
ENST00000471616.5:c.1398+120_1398+127del	ENSP00000434475.1:n.1398+120_1398+127del
ENST00000613319.4:c.952+120_952+127del	ENSP00000480522.1:n.952+120_952+127del
NM_001253727.1:c.1426+120_1426+127del	NP_001240656.1:n.1426+120_1426+127del
NM_001253728.1:c.1246+120_1246+127del	NP_001240657.1:n.1246+120_1246+127del
NM_001253729.1:c.1201+120_1201+127del	NP_001240658.1:n.1201+120_1201+127del
NM_001253730.1:c.952+120_952+127del	NP_001240659.1:n.952+120_952+127del
NM_001253732.1:c.949+120_949+127del	NP_001240661.1:n.949+120_949+127del
NM_001253733.1:c.877+120_877+127del	NP_001240662.1:n.877+120_877+127del
NM_021634.3:c.1345+120_1345+127del	NP_067647.2:n.1345+120_1345+127del
NR_045579.1:n.2225+120_2225+127del
NR_045580.1:n.1661+120_1661+127del
NR_045581.1:n.1632+120_1632+127del
NR_045582.1:n.1569+120_1569+127del
NR_045583.1:n.1548+120_1548+127del
NR_045584.1:n.1661+120_1661+127del
XM_011532174.1:c.1423+120_1423+127del	XP_011530476.1:n.1423+120_1423+127del
XM_011532175.1:c.1354+120_1354+127del	XP_011530477.1:n.1354+120_1354+127del
XM_011532176.1:c.1273+120_1273+127del	XP_011530478.1:n.1273+120_1273+127del
XM_011532177.1:c.1183+120_1183+127del	XP_011530479.1:n.1183+120_1183+127del
XM_011532178.1:c.1183+120_1183+127del	XP_011530480.1:n.1183+120_1183+127del
XM_011532179.1:c.1196+5927_1196+5934del	XP_011530481.1:n.1196+5927_1196+5934del
NM_001363776.1:c.1102+120_1102+127del	NP_001350705.1:n.1102+120_1102+127del
XM_011532176.2:c.1273+120_1273+127del	XP_011530478.1:n.1273+120_1273+127del
XM_011532179.2:c.1196+5927_1196+5934del	XP_011530481.1:n.1196+5927_1196+5934del
XM_017008517.1:c.1351+120_1351+127del	XP_016864006.1:n.1351+120_1351+127del
XM_017008518.2:c.1342+120_1342+127del	XP_016864007.1:n.1342+120_1342+127del
XM_017008519.1:c.1183+120_1183+127del	XP_016864008.1:n.1183+120_1183+127del
XM_017008520.1:c.1183+120_1183+127del	XP_016864009.1:n.1183+120_1183+127del
XM_017008522.1:c.1099+120_1099+127del	XP_016864011.1:n.1099+120_1099+127del
XM_017008523.2:c.1115+5927_1115+5934del	XP_016864012.1:n.1115+5927_1115+5934del
XM_017008524.2:c.1043+5927_1043+5934del	XP_016864013.1:n.1043+5927_1043+5934del
XM_017008525.1:c.1016+5927_1016+5934del	XP_016864014.1:n.1016+5927_1016+5934del
XM_017008526.1:c.877+120_877+127del	XP_016864015.1:n.877+120_877+127del
NM_021634.4:c.1345+120_1345+127del MANE Select	NP_067647.2:n.1345+120_1345+127del
NM_001253728.2:c.1246+120_1246+127del	NP_001240657.1:n.1246+120_1246+127del
NM_001253729.2:c.1201+120_1201+127del	NP_001240658.1:n.1201+120_1201+127del
NM_001253732.2:c.949+120_949+127del	NP_001240661.1:n.949+120_949+127del
NR_045579.2:n.2057+120_2057+127del
NR_045580.2:n.1493+120_1493+127del
NR_045581.2:n.1464+120_1464+127del
NR_045582.2:n.1401+120_1401+127del
NR_045583.2:n.1380+120_1380+127del
NR_045584.2:n.1493+120_1493+127del
NM_001253727.2:c.1426+120_1426+127del	NP_001240656.1:n.1426+120_1426+127del
NM_001253730.2:c.952+120_952+127del	NP_001240659.1:n.952+120_952+127del
NM_001253733.2:c.877+120_877+127del	NP_001240662.1:n.877+120_877+127del