Canonical Allele Identifier: CA358564160

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566266G>T (hg19) ; chr4:g.158645114G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645114G>T , CM000666.2:g.158645114G>T	GRCh38
NC_000004.11:g.159566266G>T , CM000666.1:g.159566266G>T	GRCh37
NC_000004.10:g.159785716G>T	NCBI36
NG_031835.1:g.128401G>T
NG_031835.2:g.128401G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1321G>T MANE Select	ENSP00000303248.5:p.Ala441Ser
ENST00000307765.9:c.1321G>T	ENSP00000303248.5:p.Ala441Ser
ENST00000342048.9:c.*931G>T	ENSP00000432036.1:n.*931G>T
ENST00000343542.9:c.1177G>T	ENSP00000345889.5:p.Ala393Ser
ENST00000423548.5:c.1402G>T	ENSP00000405841.2:p.Ala468Ser
ENST00000448688.6:c.853G>T	ENSP00000414885.3:p.Ala285Ser
ENST00000460056.6:c.1078G>T	ENSP00000423306.1:p.Ala360Ser
ENST00000470033.2:c.1222G>T	ENSP00000420712.1:p.Ala408Ser
ENST00000471616.5:c.1374G>T	ENSP00000434475.1:n.1374G>T
ENST00000613319.4:c.928G>T	ENSP00000480522.1:p.Ala310Ser
NM_001253727.1:c.1402G>T	NP_001240656.1:p.Ala468Ser
NM_001253728.1:c.1222G>T	NP_001240657.1:p.Ala408Ser
NM_001253729.1:c.1177G>T	NP_001240658.1:p.Ala393Ser
NM_001253730.1:c.928G>T	NP_001240659.1:p.Ala310Ser
NM_001253732.1:c.925G>T	NP_001240661.1:p.Ala309Ser
NM_001253733.1:c.853G>T	NP_001240662.1:p.Ala285Ser
NM_021634.3:c.1321G>T	NP_067647.2:p.Ala441Ser
NR_045579.1:n.2201G>T
NR_045580.1:n.1637G>T
NR_045581.1:n.1608G>T
NR_045582.1:n.1545G>T
NR_045583.1:n.1524G>T
NR_045584.1:n.1637G>T
XM_011532174.1:c.1399G>T	XP_011530476.1:p.Ala467Ser
XM_011532175.1:c.1330G>T	XP_011530477.1:p.Ala444Ser
XM_011532176.1:c.1249G>T	XP_011530478.1:p.Ala417Ser
XM_011532177.1:c.1159G>T	XP_011530479.1:p.Ala387Ser
XM_011532178.1:c.1159G>T	XP_011530480.1:p.Ala387Ser
XM_011532179.1:c.1196+5783G>T	XP_011530481.1:n.1196+5783G>T
NM_001363776.1:c.1078G>T	NP_001350705.1:p.Ala360Ser
XM_011532176.2:c.1249G>T	XP_011530478.1:p.Ala417Ser
XM_011532179.2:c.1196+5783G>T	XP_011530481.1:n.1196+5783G>T
XM_017008517.1:c.1327G>T	XP_016864006.1:p.Ala443Ser
XM_017008518.2:c.1318G>T	XP_016864007.1:p.Ala440Ser
XM_017008519.1:c.1159G>T	XP_016864008.1:p.Ala387Ser
XM_017008520.1:c.1159G>T	XP_016864009.1:p.Ala387Ser
XM_017008522.1:c.1075G>T	XP_016864011.1:p.Ala359Ser
XM_017008523.2:c.1115+5783G>T	XP_016864012.1:n.1115+5783G>T
XM_017008524.2:c.1043+5783G>T	XP_016864013.1:n.1043+5783G>T
XM_017008525.1:c.1016+5783G>T	XP_016864014.1:n.1016+5783G>T
XM_017008526.1:c.853G>T	XP_016864015.1:p.Ala285Ser
NM_021634.4:c.1321G>T MANE Select	NP_067647.2:p.Ala441Ser
NM_001253728.2:c.1222G>T	NP_001240657.1:p.Ala408Ser
NM_001253729.2:c.1177G>T	NP_001240658.1:p.Ala393Ser
NM_001253732.2:c.925G>T	NP_001240661.1:p.Ala309Ser
NR_045579.2:n.2033G>T
NR_045580.2:n.1469G>T
NR_045581.2:n.1440G>T
NR_045582.2:n.1377G>T
NR_045583.2:n.1356G>T
NR_045584.2:n.1469G>T
NM_001253727.2:c.1402G>T	NP_001240656.1:p.Ala468Ser
NM_001253730.2:c.928G>T	NP_001240659.1:p.Ala310Ser
NM_001253733.2:c.853G>T	NP_001240662.1:p.Ala285Ser