Canonical Allele Identifier: CA442140352

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566250T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645098T>C , CM000666.2:g.158645098T>C	GRCh38
NC_000004.11:g.159566250T>C , CM000666.1:g.159566250T>C	GRCh37
NC_000004.10:g.159785700T>C	NCBI36
NG_031835.1:g.128385T>C
NG_031835.2:g.128385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1305T>C MANE Select	ENSP00000303248.5:p.Ser435=
ENST00000307765.9:c.1305T>C	ENSP00000303248.5:p.Ser435=
ENST00000342048.9:c.*915T>C	ENSP00000432036.1:n.*915T>C
ENST00000343542.9:c.1161T>C	ENSP00000345889.5:p.Ser387=
ENST00000423548.5:c.1386T>C	ENSP00000405841.2:p.Ser462=
ENST00000448688.6:c.837T>C	ENSP00000414885.3:p.Ser279=
ENST00000460056.6:c.1062T>C	ENSP00000423306.1:p.Ser354=
ENST00000470033.2:c.1206T>C	ENSP00000420712.1:p.Ser402=
ENST00000471616.5:c.1358T>C	ENSP00000434475.1:n.1358T>C
ENST00000613319.4:c.912T>C	ENSP00000480522.1:p.Ser304=
NM_001253727.1:c.1386T>C	NP_001240656.1:p.Ser462=
NM_001253728.1:c.1206T>C	NP_001240657.1:p.Ser402=
NM_001253729.1:c.1161T>C	NP_001240658.1:p.Ser387=
NM_001253730.1:c.912T>C	NP_001240659.1:p.Ser304=
NM_001253732.1:c.909T>C	NP_001240661.1:p.Ser303=
NM_001253733.1:c.837T>C	NP_001240662.1:p.Ser279=
NM_021634.3:c.1305T>C	NP_067647.2:p.Ser435=
NR_045579.1:n.2185T>C
NR_045580.1:n.1621T>C
NR_045581.1:n.1592T>C
NR_045582.1:n.1529T>C
NR_045583.1:n.1508T>C
NR_045584.1:n.1621T>C
XM_011532174.1:c.1383T>C	XP_011530476.1:p.Ser461=
XM_011532175.1:c.1314T>C	XP_011530477.1:p.Ser438=
XM_011532176.1:c.1233T>C	XP_011530478.1:p.Ser411=
XM_011532177.1:c.1143T>C	XP_011530479.1:p.Ser381=
XM_011532178.1:c.1143T>C	XP_011530480.1:p.Ser381=
XM_011532179.1:c.1196+5767T>C	XP_011530481.1:n.1196+5767T>C
NM_001363776.1:c.1062T>C	NP_001350705.1:p.Ser354=
XM_011532176.2:c.1233T>C	XP_011530478.1:p.Ser411=
XM_011532179.2:c.1196+5767T>C	XP_011530481.1:n.1196+5767T>C
XM_017008517.1:c.1311T>C	XP_016864006.1:p.Ser437=
XM_017008518.2:c.1302T>C	XP_016864007.1:p.Ser434=
XM_017008519.1:c.1143T>C	XP_016864008.1:p.Ser381=
XM_017008520.1:c.1143T>C	XP_016864009.1:p.Ser381=
XM_017008522.1:c.1059T>C	XP_016864011.1:p.Ser353=
XM_017008523.2:c.1115+5767T>C	XP_016864012.1:n.1115+5767T>C
XM_017008524.2:c.1043+5767T>C	XP_016864013.1:n.1043+5767T>C
XM_017008525.1:c.1016+5767T>C	XP_016864014.1:n.1016+5767T>C
XM_017008526.1:c.837T>C	XP_016864015.1:p.Ser279=
NM_021634.4:c.1305T>C MANE Select	NP_067647.2:p.Ser435=
NM_001253728.2:c.1206T>C	NP_001240657.1:p.Ser402=
NM_001253729.2:c.1161T>C	NP_001240658.1:p.Ser387=
NM_001253732.2:c.909T>C	NP_001240661.1:p.Ser303=
NR_045579.2:n.2017T>C
NR_045580.2:n.1453T>C
NR_045581.2:n.1424T>C
NR_045582.2:n.1361T>C
NR_045583.2:n.1340T>C
NR_045584.2:n.1453T>C
NM_001253727.2:c.1386T>C	NP_001240656.1:p.Ser462=
NM_001253730.2:c.912T>C	NP_001240659.1:p.Ser304=
NM_001253733.2:c.837T>C	NP_001240662.1:p.Ser279=