Canonical Allele Identifier: CA357404573

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832843G>A (hg19) ; chr4:g.78911689G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911689G>A , CM000666.2:g.78911689G>A	GRCh38
NC_000004.11:g.79832843G>A , CM000666.1:g.79832843G>A	GRCh37
NC_000004.10:g.80051867G>A	NCBI36
NG_047162.1:g.140312G>A
NG_053104.1:g.32750C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3142G>A (BMP2K) MANE Select	ENSP00000424668.2:p.Ala1048Thr
ENST00000335016.9:c.3142G>A (BMP2K)	ENSP00000334836.5:p.Ala1048Thr
ENST00000342820.10:c.*782+3521C>T (PAQR3)	ENSP00000344203.6:n.*782+3521C>T
ENST00000502613.1:c.2219G>A (BMP2K)
ENST00000511594.5:c.*500C>T (PAQR3)	ENSP00000425080.1:n.*500C>T
ENST00000512760.5:c.*792+3521C>T (PAQR3)	ENSP00000426875.1:n.*792+3521C>T
ENST00000628286.1:c.*2118G>A (BMP2K)	ENSP00000487317.1:n.*2118G>A
NM_198892.1:c.3142G>A (BMP2K)	NP_942595.1:p.Ala1048Thr
XM_005263117.1:c.3031G>A (BMP2K)	XP_005263174.1:p.Ala1011Thr
XM_011532101.1:c.2902G>A (BMP2K)	XP_011530403.1:p.Ala968Thr
XR_938694.1:n.1118-5528C>T (PAQR3)
XM_017008381.1:c.2902G>A (BMP2K)	XP_016863870.1:p.Ala968Thr
XM_017008382.1:c.2254G>A (BMP2K)	XP_016863871.1:p.Ala752Thr
XR_938694.3:n.1098-5528C>T (PAQR3)
NM_198892.2:c.3142G>A (BMP2K) MANE Select	NP_942595.1:p.Ala1048Thr