Canonical Allele Identifier: CA789734649

Gene: RXFP1

Linked Data

• dbSNP Id: rs1480408640
• gnomAD v4: 4-158645240-AT-A
• MyVariant Identifiers: chr4:g.159566393del (hg19) ; chr4:g.158645241del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645245del , CM000666.2:g.158645245del	GRCh38
NC_000004.11:g.159566397del , CM000666.1:g.159566397del	GRCh37
NC_000004.10:g.159785847del	NCBI36
NG_031835.1:g.128532del
NG_031835.2:g.128532del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+107del MANE Select	ENSP00000303248.5:n.1345+107del
ENST00000307765.9:c.1345+107del	ENSP00000303248.5:n.1345+107del
ENST00000342048.9:c.*955+107del	ENSP00000432036.1:n.*955+107del
ENST00000343542.9:c.1201+107del	ENSP00000345889.5:n.1201+107del
ENST00000423548.5:c.1426+107del	ENSP00000405841.2:n.1426+107del
ENST00000448688.6:c.877+107del	ENSP00000414885.3:n.877+107del
ENST00000460056.6:c.1102+107del	ENSP00000423306.1:n.1102+107del
ENST00000470033.2:c.1246+107del	ENSP00000420712.1:n.1246+107del
ENST00000471616.5:c.1398+107del	ENSP00000434475.1:n.1398+107del
ENST00000613319.4:c.952+107del	ENSP00000480522.1:n.952+107del
NM_001253727.1:c.1426+107del	NP_001240656.1:n.1426+107del
NM_001253728.1:c.1246+107del	NP_001240657.1:n.1246+107del
NM_001253729.1:c.1201+107del	NP_001240658.1:n.1201+107del
NM_001253730.1:c.952+107del	NP_001240659.1:n.952+107del
NM_001253732.1:c.949+107del	NP_001240661.1:n.949+107del
NM_001253733.1:c.877+107del	NP_001240662.1:n.877+107del
NM_021634.3:c.1345+107del	NP_067647.2:n.1345+107del
NR_045579.1:n.2225+107del
NR_045580.1:n.1661+107del
NR_045581.1:n.1632+107del
NR_045582.1:n.1569+107del
NR_045583.1:n.1548+107del
NR_045584.1:n.1661+107del
XM_011532174.1:c.1423+107del	XP_011530476.1:n.1423+107del
XM_011532175.1:c.1354+107del	XP_011530477.1:n.1354+107del
XM_011532176.1:c.1273+107del	XP_011530478.1:n.1273+107del
XM_011532177.1:c.1183+107del	XP_011530479.1:n.1183+107del
XM_011532178.1:c.1183+107del	XP_011530480.1:n.1183+107del
XM_011532179.1:c.1196+5914del	XP_011530481.1:n.1196+5914del
NM_001363776.1:c.1102+107del	NP_001350705.1:n.1102+107del
XM_011532176.2:c.1273+107del	XP_011530478.1:n.1273+107del
XM_011532179.2:c.1196+5914del	XP_011530481.1:n.1196+5914del
XM_017008517.1:c.1351+107del	XP_016864006.1:n.1351+107del
XM_017008518.2:c.1342+107del	XP_016864007.1:n.1342+107del
XM_017008519.1:c.1183+107del	XP_016864008.1:n.1183+107del
XM_017008520.1:c.1183+107del	XP_016864009.1:n.1183+107del
XM_017008522.1:c.1099+107del	XP_016864011.1:n.1099+107del
XM_017008523.2:c.1115+5914del	XP_016864012.1:n.1115+5914del
XM_017008524.2:c.1043+5914del	XP_016864013.1:n.1043+5914del
XM_017008525.1:c.1016+5914del	XP_016864014.1:n.1016+5914del
XM_017008526.1:c.877+107del	XP_016864015.1:n.877+107del
NM_021634.4:c.1345+107del MANE Select	NP_067647.2:n.1345+107del
NM_001253728.2:c.1246+107del	NP_001240657.1:n.1246+107del
NM_001253729.2:c.1201+107del	NP_001240658.1:n.1201+107del
NM_001253732.2:c.949+107del	NP_001240661.1:n.949+107del
NR_045579.2:n.2057+107del
NR_045580.2:n.1493+107del
NR_045581.2:n.1464+107del
NR_045582.2:n.1401+107del
NR_045583.2:n.1380+107del
NR_045584.2:n.1493+107del
NM_001253727.2:c.1426+107del	NP_001240656.1:n.1426+107del
NM_001253730.2:c.952+107del	NP_001240659.1:n.952+107del
NM_001253733.2:c.877+107del	NP_001240662.1:n.877+107del