Canonical Allele Identifier: CA2082576987

Gene: RXFP2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31777398A= , CM000675.2:g.31777398A=	GRCh38
NC_000013.10:g.32351535A= , CM000675.1:g.32351535A=	GRCh37
NC_000013.9:g.31249535A=	NCBI36
NG_015819.1:g.42857A=

Transcript Alleles

HGVS	Amino-acid Change
NM_130806.5:c.664A= MANE Select	NP_570718.1:p.Thr222=
ENST00000298386.7:c.664A= MANE Select	ENSP00000298386.2:p.Thr222=
NM_001166058.1:c.664A=	NP_001159530.1:p.Thr222=
NM_001166058.2:c.664A=	NP_001159530.1:p.Thr222=
NM_130806.3:c.664A=	NP_570718.1:p.Thr222=
NM_130806.4:c.664A=	NP_570718.1:p.Thr222=
ENST00000298386.6:c.664A=	ENSP00000298386.2:p.Thr222=
ENST00000380314.2:c.664A=	ENSP00000369670.1:p.Thr222=
XM_011534918.1:c.664A=	XP_011533220.1:p.Thr222=
XM_017020389.1:c.664A=	XP_016875878.1:p.Thr222=