Canonical Allele Identifier: CA2347441769

Gene: PROKR2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5314314T= , CM000682.2:g.5314314T=	GRCh38
NC_000020.10:g.5294960T= , CM000682.1:g.5294960T=	GRCh37
NC_000020.9:g.5242960T=	NCBI36
NG_008132.1:g.5056A=
NG_008132.2:g.5056A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217270.4:c.56A=	ENSP00000217270.3:p.Asp19=
ENST00000678059.1:c.-22-31A=	ENSP00000503366.1:n.-22-31A=
ENST00000678254.1:c.56A= MANE Select	ENSP00000504128.1:p.Asp19=
ENST00000217270.3:c.56A=	ENSP00000217270.3:p.Asp19=
NM_144773.2:c.56A=	NP_658986.1:p.Asp19=
XM_005260663.2:c.56A=	XP_005260720.1:p.Asp19=
XM_011529159.1:c.-22-31A=	XP_011527461.1:n.-22-31A=
NM_144773.3:c.56A=	NP_658986.1:p.Asp19=
XM_017027646.1:c.56A=	XP_016883135.1:p.Asp19=
NM_144773.4:c.56A= MANE Select	NP_658986.1:p.Asp19=