Canonical Allele Identifier: CA442140386

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566277C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645125C>T , CM000666.2:g.158645125C>T	GRCh38
NC_000004.11:g.159566277C>T , CM000666.1:g.159566277C>T	GRCh37
NC_000004.10:g.159785727C>T	NCBI36
NG_031835.1:g.128412C>T
NG_031835.2:g.128412C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1332C>T MANE Select	ENSP00000303248.5:p.Ile444=
ENST00000307765.9:c.1332C>T	ENSP00000303248.5:p.Ile444=
ENST00000342048.9:c.*942C>T	ENSP00000432036.1:n.*942C>T
ENST00000343542.9:c.1188C>T	ENSP00000345889.5:p.Ile396=
ENST00000423548.5:c.1413C>T	ENSP00000405841.2:p.Ile471=
ENST00000448688.6:c.864C>T	ENSP00000414885.3:p.Ile288=
ENST00000460056.6:c.1089C>T	ENSP00000423306.1:p.Ile363=
ENST00000470033.2:c.1233C>T	ENSP00000420712.1:p.Ile411=
ENST00000471616.5:c.1385C>T	ENSP00000434475.1:n.1385C>T
ENST00000613319.4:c.939C>T	ENSP00000480522.1:p.Ile313=
NM_001253727.1:c.1413C>T	NP_001240656.1:p.Ile471=
NM_001253728.1:c.1233C>T	NP_001240657.1:p.Ile411=
NM_001253729.1:c.1188C>T	NP_001240658.1:p.Ile396=
NM_001253730.1:c.939C>T	NP_001240659.1:p.Ile313=
NM_001253732.1:c.936C>T	NP_001240661.1:p.Ile312=
NM_001253733.1:c.864C>T	NP_001240662.1:p.Ile288=
NM_021634.3:c.1332C>T	NP_067647.2:p.Ile444=
NR_045579.1:n.2212C>T
NR_045580.1:n.1648C>T
NR_045581.1:n.1619C>T
NR_045582.1:n.1556C>T
NR_045583.1:n.1535C>T
NR_045584.1:n.1648C>T
XM_011532174.1:c.1410C>T	XP_011530476.1:p.Ile470=
XM_011532175.1:c.1341C>T	XP_011530477.1:p.Ile447=
XM_011532176.1:c.1260C>T	XP_011530478.1:p.Ile420=
XM_011532177.1:c.1170C>T	XP_011530479.1:p.Ile390=
XM_011532178.1:c.1170C>T	XP_011530480.1:p.Ile390=
XM_011532179.1:c.1196+5794C>T	XP_011530481.1:n.1196+5794C>T
NM_001363776.1:c.1089C>T	NP_001350705.1:p.Ile363=
XM_011532176.2:c.1260C>T	XP_011530478.1:p.Ile420=
XM_011532179.2:c.1196+5794C>T	XP_011530481.1:n.1196+5794C>T
XM_017008517.1:c.1338C>T	XP_016864006.1:p.Ile446=
XM_017008518.2:c.1329C>T	XP_016864007.1:p.Ile443=
XM_017008519.1:c.1170C>T	XP_016864008.1:p.Ile390=
XM_017008520.1:c.1170C>T	XP_016864009.1:p.Ile390=
XM_017008522.1:c.1086C>T	XP_016864011.1:p.Ile362=
XM_017008523.2:c.1115+5794C>T	XP_016864012.1:n.1115+5794C>T
XM_017008524.2:c.1043+5794C>T	XP_016864013.1:n.1043+5794C>T
XM_017008525.1:c.1016+5794C>T	XP_016864014.1:n.1016+5794C>T
XM_017008526.1:c.864C>T	XP_016864015.1:p.Ile288=
NM_021634.4:c.1332C>T MANE Select	NP_067647.2:p.Ile444=
NM_001253728.2:c.1233C>T	NP_001240657.1:p.Ile411=
NM_001253729.2:c.1188C>T	NP_001240658.1:p.Ile396=
NM_001253732.2:c.936C>T	NP_001240661.1:p.Ile312=
NR_045579.2:n.2044C>T
NR_045580.2:n.1480C>T
NR_045581.2:n.1451C>T
NR_045582.2:n.1388C>T
NR_045583.2:n.1367C>T
NR_045584.2:n.1480C>T
NM_001253727.2:c.1413C>T	NP_001240656.1:p.Ile471=
NM_001253730.2:c.939C>T	NP_001240659.1:p.Ile313=
NM_001253733.2:c.864C>T	NP_001240662.1:p.Ile288=