Canonical Allele Identifier: CA2347441729

Gene: PROKR2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5314230C= , CM000682.2:g.5314230C=	GRCh38
NC_000020.10:g.5294876C= , CM000682.1:g.5294876C=	GRCh37
NC_000020.9:g.5242876C=	NCBI36
NG_008132.1:g.5140G=
NG_008132.2:g.5140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217270.4:c.140G=	ENSP00000217270.3:p.Arg47=
ENST00000678059.1:c.32G=	ENSP00000503366.1:p.Arg11=
ENST00000678254.1:c.140G= MANE Select	ENSP00000504128.1:p.Arg47=
ENST00000217270.3:c.140G=	ENSP00000217270.3:p.Arg47=
NM_144773.2:c.140G=	NP_658986.1:p.Arg47=
XM_005260663.2:c.140G=	XP_005260720.1:p.Arg47=
XM_011529159.1:c.32G=	XP_011527461.1:p.Arg11=
NM_144773.3:c.140G=	NP_658986.1:p.Arg47=
XM_017027646.1:c.140G=	XP_016883135.1:p.Arg47=
NM_144773.4:c.140G= MANE Select	NP_658986.1:p.Arg47=