Canonical Allele Identifier: CA408168351

Gene: PROKR2

Linked Data

• MyVariant Identifiers: chr20:g.5294895C>A (hg19) ; chr20:g.5314249C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5314249C>A , CM000682.2:g.5314249C>A	GRCh38
NC_000020.10:g.5294895C>A , CM000682.1:g.5294895C>A	GRCh37
NC_000020.9:g.5242895C>A	NCBI36
NG_008132.1:g.5121G>T
NG_008132.2:g.5121G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217270.4:c.121G>T	ENSP00000217270.3:p.Glu41Ter
ENST00000678059.1:c.13G>T	ENSP00000503366.1:p.Glu5Ter
ENST00000678254.1:c.121G>T MANE Select	ENSP00000504128.1:p.Glu41Ter
ENST00000217270.3:c.121G>T	ENSP00000217270.3:p.Glu41Ter
NM_144773.2:c.121G>T	NP_658986.1:p.Glu41Ter
XM_005260663.2:c.121G>T	XP_005260720.1:p.Glu41Ter
XM_011529159.1:c.13G>T	XP_011527461.1:p.Glu5Ter
NM_144773.3:c.121G>T	NP_658986.1:p.Glu41Ter
XM_017027646.1:c.121G>T	XP_016883135.1:p.Glu41Ter
NM_144773.4:c.121G>T MANE Select	NP_658986.1:p.Glu41Ter