Canonical Allele Identifier: CA358564154

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566264A>C (hg19) ; chr4:g.158645112A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645112A>C , CM000666.2:g.158645112A>C	GRCh38
NC_000004.11:g.159566264A>C , CM000666.1:g.159566264A>C	GRCh37
NC_000004.10:g.159785714A>C	NCBI36
NG_031835.1:g.128399A>C
NG_031835.2:g.128399A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1319A>C MANE Select	ENSP00000303248.5:p.Tyr440Ser
ENST00000307765.9:c.1319A>C	ENSP00000303248.5:p.Tyr440Ser
ENST00000342048.9:c.*929A>C	ENSP00000432036.1:n.*929A>C
ENST00000343542.9:c.1175A>C	ENSP00000345889.5:p.Tyr392Ser
ENST00000423548.5:c.1400A>C	ENSP00000405841.2:p.Tyr467Ser
ENST00000448688.6:c.851A>C	ENSP00000414885.3:p.Tyr284Ser
ENST00000460056.6:c.1076A>C	ENSP00000423306.1:p.Tyr359Ser
ENST00000470033.2:c.1220A>C	ENSP00000420712.1:p.Tyr407Ser
ENST00000471616.5:c.1372A>C	ENSP00000434475.1:n.1372A>C
ENST00000613319.4:c.926A>C	ENSP00000480522.1:p.Tyr309Ser
NM_001253727.1:c.1400A>C	NP_001240656.1:p.Tyr467Ser
NM_001253728.1:c.1220A>C	NP_001240657.1:p.Tyr407Ser
NM_001253729.1:c.1175A>C	NP_001240658.1:p.Tyr392Ser
NM_001253730.1:c.926A>C	NP_001240659.1:p.Tyr309Ser
NM_001253732.1:c.923A>C	NP_001240661.1:p.Tyr308Ser
NM_001253733.1:c.851A>C	NP_001240662.1:p.Tyr284Ser
NM_021634.3:c.1319A>C	NP_067647.2:p.Tyr440Ser
NR_045579.1:n.2199A>C
NR_045580.1:n.1635A>C
NR_045581.1:n.1606A>C
NR_045582.1:n.1543A>C
NR_045583.1:n.1522A>C
NR_045584.1:n.1635A>C
XM_011532174.1:c.1397A>C	XP_011530476.1:p.Tyr466Ser
XM_011532175.1:c.1328A>C	XP_011530477.1:p.Tyr443Ser
XM_011532176.1:c.1247A>C	XP_011530478.1:p.Tyr416Ser
XM_011532177.1:c.1157A>C	XP_011530479.1:p.Tyr386Ser
XM_011532178.1:c.1157A>C	XP_011530480.1:p.Tyr386Ser
XM_011532179.1:c.1196+5781A>C	XP_011530481.1:n.1196+5781A>C
NM_001363776.1:c.1076A>C	NP_001350705.1:p.Tyr359Ser
XM_011532176.2:c.1247A>C	XP_011530478.1:p.Tyr416Ser
XM_011532179.2:c.1196+5781A>C	XP_011530481.1:n.1196+5781A>C
XM_017008517.1:c.1325A>C	XP_016864006.1:p.Tyr442Ser
XM_017008518.2:c.1316A>C	XP_016864007.1:p.Tyr439Ser
XM_017008519.1:c.1157A>C	XP_016864008.1:p.Tyr386Ser
XM_017008520.1:c.1157A>C	XP_016864009.1:p.Tyr386Ser
XM_017008522.1:c.1073A>C	XP_016864011.1:p.Tyr358Ser
XM_017008523.2:c.1115+5781A>C	XP_016864012.1:n.1115+5781A>C
XM_017008524.2:c.1043+5781A>C	XP_016864013.1:n.1043+5781A>C
XM_017008525.1:c.1016+5781A>C	XP_016864014.1:n.1016+5781A>C
XM_017008526.1:c.851A>C	XP_016864015.1:p.Tyr284Ser
NM_021634.4:c.1319A>C MANE Select	NP_067647.2:p.Tyr440Ser
NM_001253728.2:c.1220A>C	NP_001240657.1:p.Tyr407Ser
NM_001253729.2:c.1175A>C	NP_001240658.1:p.Tyr392Ser
NM_001253732.2:c.923A>C	NP_001240661.1:p.Tyr308Ser
NR_045579.2:n.2031A>C
NR_045580.2:n.1467A>C
NR_045581.2:n.1438A>C
NR_045582.2:n.1375A>C
NR_045583.2:n.1354A>C
NR_045584.2:n.1467A>C
NM_001253727.2:c.1400A>C	NP_001240656.1:p.Tyr467Ser
NM_001253730.2:c.926A>C	NP_001240659.1:p.Tyr309Ser
NM_001253733.2:c.851A>C	NP_001240662.1:p.Tyr284Ser