Canonical Allele Identifier: CA2672509917

Gene: RXFP1

Linked Data

• gnomAD v4: 4-158645137-CTGTGAGTATTTCCTGGTTAAAGGAGAATTGTAGTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645140_158645175del , CM000666.2:g.158645140_158645175del	GRCh38
NC_000004.11:g.159566292_159566327del , CM000666.1:g.159566292_159566327del	GRCh37
NC_000004.10:g.159785742_159785777del	NCBI36
NG_031835.1:g.128427_128462del
NG_031835.2:g.128427_128462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+2_1345+37del
ENST00000307765.9:c.1345+2_1345+37del
ENST00000342048.9:c.*955+2_*955+37del
ENST00000343542.9:c.1201+2_1201+37del
ENST00000423548.5:c.1426+2_1426+37del
ENST00000448688.6:c.877+2_877+37del
ENST00000460056.6:c.1102+2_1102+37del
ENST00000470033.2:c.1246+2_1246+37del
ENST00000471616.5:c.1398+2_1398+37del
ENST00000613319.4:c.952+2_952+37del
NM_001253727.1:c.1426+2_1426+37del
NM_001253728.1:c.1246+2_1246+37del
NM_001253729.1:c.1201+2_1201+37del
NM_001253730.1:c.952+2_952+37del
NM_001253732.1:c.949+2_949+37del
NM_001253733.1:c.877+2_877+37del
NM_021634.3:c.1345+2_1345+37del
NR_045579.1:n.2225+2_2225+37del
NR_045580.1:n.1661+2_1661+37del
NR_045581.1:n.1632+2_1632+37del
NR_045582.1:n.1569+2_1569+37del
NR_045583.1:n.1548+2_1548+37del
NR_045584.1:n.1661+2_1661+37del
XM_011532174.1:c.1423+2_1423+37del
XM_011532175.1:c.1354+2_1354+37del
XM_011532176.1:c.1273+2_1273+37del
XM_011532177.1:c.1183+2_1183+37del
XM_011532178.1:c.1183+2_1183+37del
XM_011532179.1:c.1196+5809_1196+5844del	XP_011530481.1:n.1196+5809_1196+5844del
NM_001363776.1:c.1102+2_1102+37del
XM_011532176.2:c.1273+2_1273+37del
XM_011532179.2:c.1196+5809_1196+5844del	XP_011530481.1:n.1196+5809_1196+5844del
XM_017008517.1:c.1351+2_1351+37del
XM_017008518.2:c.1342+2_1342+37del
XM_017008519.1:c.1183+2_1183+37del
XM_017008520.1:c.1183+2_1183+37del
XM_017008522.1:c.1099+2_1099+37del
XM_017008523.2:c.1115+5809_1115+5844del	XP_016864012.1:n.1115+5809_1115+5844del
XM_017008524.2:c.1043+5809_1043+5844del	XP_016864013.1:n.1043+5809_1043+5844del
XM_017008525.1:c.1016+5809_1016+5844del	XP_016864014.1:n.1016+5809_1016+5844del
XM_017008526.1:c.877+2_877+37del
NM_021634.4:c.1345+2_1345+37del
NM_001253728.2:c.1246+2_1246+37del
NM_001253729.2:c.1201+2_1201+37del
NM_001253732.2:c.949+2_949+37del
NR_045579.2:n.2057+2_2057+37del
NR_045580.2:n.1493+2_1493+37del
NR_045581.2:n.1464+2_1464+37del
NR_045582.2:n.1401+2_1401+37del
NR_045583.2:n.1380+2_1380+37del
NR_045584.2:n.1493+2_1493+37del
NM_001253727.2:c.1426+2_1426+37del
NM_001253730.2:c.952+2_952+37del
NM_001253733.2:c.877+2_877+37del