Canonical Allele Identifier: CA358564172

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566271G>C (hg19) ; chr4:g.158645119G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645119G>C , CM000666.2:g.158645119G>C	GRCh38
NC_000004.11:g.159566271G>C , CM000666.1:g.159566271G>C	GRCh37
NC_000004.10:g.159785721G>C	NCBI36
NG_031835.1:g.128406G>C
NG_031835.2:g.128406G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1326G>C MANE Select	ENSP00000303248.5:p.Met442Ile
ENST00000307765.9:c.1326G>C	ENSP00000303248.5:p.Met442Ile
ENST00000342048.9:c.*936G>C	ENSP00000432036.1:n.*936G>C
ENST00000343542.9:c.1182G>C	ENSP00000345889.5:p.Met394Ile
ENST00000423548.5:c.1407G>C	ENSP00000405841.2:p.Met469Ile
ENST00000448688.6:c.858G>C	ENSP00000414885.3:p.Met286Ile
ENST00000460056.6:c.1083G>C	ENSP00000423306.1:p.Met361Ile
ENST00000470033.2:c.1227G>C	ENSP00000420712.1:p.Met409Ile
ENST00000471616.5:c.1379G>C	ENSP00000434475.1:n.1379G>C
ENST00000613319.4:c.933G>C	ENSP00000480522.1:p.Met311Ile
NM_001253727.1:c.1407G>C	NP_001240656.1:p.Met469Ile
NM_001253728.1:c.1227G>C	NP_001240657.1:p.Met409Ile
NM_001253729.1:c.1182G>C	NP_001240658.1:p.Met394Ile
NM_001253730.1:c.933G>C	NP_001240659.1:p.Met311Ile
NM_001253732.1:c.930G>C	NP_001240661.1:p.Met310Ile
NM_001253733.1:c.858G>C	NP_001240662.1:p.Met286Ile
NM_021634.3:c.1326G>C	NP_067647.2:p.Met442Ile
NR_045579.1:n.2206G>C
NR_045580.1:n.1642G>C
NR_045581.1:n.1613G>C
NR_045582.1:n.1550G>C
NR_045583.1:n.1529G>C
NR_045584.1:n.1642G>C
XM_011532174.1:c.1404G>C	XP_011530476.1:p.Met468Ile
XM_011532175.1:c.1335G>C	XP_011530477.1:p.Met445Ile
XM_011532176.1:c.1254G>C	XP_011530478.1:p.Met418Ile
XM_011532177.1:c.1164G>C	XP_011530479.1:p.Met388Ile
XM_011532178.1:c.1164G>C	XP_011530480.1:p.Met388Ile
XM_011532179.1:c.1196+5788G>C	XP_011530481.1:n.1196+5788G>C
NM_001363776.1:c.1083G>C	NP_001350705.1:p.Met361Ile
XM_011532176.2:c.1254G>C	XP_011530478.1:p.Met418Ile
XM_011532179.2:c.1196+5788G>C	XP_011530481.1:n.1196+5788G>C
XM_017008517.1:c.1332G>C	XP_016864006.1:p.Met444Ile
XM_017008518.2:c.1323G>C	XP_016864007.1:p.Met441Ile
XM_017008519.1:c.1164G>C	XP_016864008.1:p.Met388Ile
XM_017008520.1:c.1164G>C	XP_016864009.1:p.Met388Ile
XM_017008522.1:c.1080G>C	XP_016864011.1:p.Met360Ile
XM_017008523.2:c.1115+5788G>C	XP_016864012.1:n.1115+5788G>C
XM_017008524.2:c.1043+5788G>C	XP_016864013.1:n.1043+5788G>C
XM_017008525.1:c.1016+5788G>C	XP_016864014.1:n.1016+5788G>C
XM_017008526.1:c.858G>C	XP_016864015.1:p.Met286Ile
NM_021634.4:c.1326G>C MANE Select	NP_067647.2:p.Met442Ile
NM_001253728.2:c.1227G>C	NP_001240657.1:p.Met409Ile
NM_001253729.2:c.1182G>C	NP_001240658.1:p.Met394Ile
NM_001253732.2:c.930G>C	NP_001240661.1:p.Met310Ile
NR_045579.2:n.2038G>C
NR_045580.2:n.1474G>C
NR_045581.2:n.1445G>C
NR_045582.2:n.1382G>C
NR_045583.2:n.1361G>C
NR_045584.2:n.1474G>C
NM_001253727.2:c.1407G>C	NP_001240656.1:p.Met469Ile
NM_001253730.2:c.933G>C	NP_001240659.1:p.Met311Ile
NM_001253733.2:c.858G>C	NP_001240662.1:p.Met286Ile