Canonical Allele Identifier: CA1470756850

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911785T= , CM000666.2:g.78911785T=	GRCh38
NC_000004.11:g.79832939T= , CM000666.1:g.79832939T=	GRCh37
NC_000004.10:g.80051963T=	NCBI36
NG_047162.1:g.140408T=
NG_053104.1:g.32654A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3238T= (BMP2K) MANE Select	ENSP00000424668.2:p.Ser1080=
ENST00000335016.9:c.3238T= (BMP2K)	ENSP00000334836.5:p.Ser1080=
ENST00000342820.10:c.*782+3425A= (PAQR3)	ENSP00000344203.6:n.*782+3425A=
ENST00000502613.1:c.2315T= (BMP2K)
ENST00000511594.5:c.*404A= (PAQR3)	ENSP00000425080.1:n.*404A=
ENST00000512760.5:c.*792+3425A= (PAQR3)	ENSP00000426875.1:n.*792+3425A=
ENST00000628286.1:c.*2214T= (BMP2K)	ENSP00000487317.1:n.*2214T=
NM_198892.1:c.3238T= (BMP2K)	NP_942595.1:p.Ser1080=
XM_005263117.1:c.3127T= (BMP2K)	XP_005263174.1:p.Ser1043=
XM_011532101.1:c.2998T= (BMP2K)	XP_011530403.1:p.Ser1000=
XR_938694.1:n.1118-5624A= (PAQR3)
XM_017008381.1:c.2998T= (BMP2K)	XP_016863870.1:p.Ser1000=
XM_017008382.1:c.2350T= (BMP2K)	XP_016863871.1:p.Ser784=
XR_938694.3:n.1098-5624A= (PAQR3)
NM_198892.2:c.3238T= (BMP2K) MANE Select	NP_942595.1:p.Ser1080=