Canonical Allele Identifier: CA1470756836

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911755G= , CM000666.2:g.78911755G=	GRCh38
NC_000004.11:g.79832909G= , CM000666.1:g.79832909G=	GRCh37
NC_000004.10:g.80051933G=	NCBI36
NG_047162.1:g.140378G=
NG_053104.1:g.32684C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3208G= (BMP2K) MANE Select	ENSP00000424668.2:p.Gly1070=
ENST00000335016.9:c.3208G= (BMP2K)	ENSP00000334836.5:p.Gly1070=
ENST00000342820.10:c.*782+3455C= (PAQR3)	ENSP00000344203.6:n.*782+3455C=
ENST00000502613.1:c.2285G= (BMP2K)
ENST00000511594.5:c.*434C= (PAQR3)	ENSP00000425080.1:n.*434C=
ENST00000512760.5:c.*792+3455C= (PAQR3)	ENSP00000426875.1:n.*792+3455C=
ENST00000628286.1:c.*2184G= (BMP2K)	ENSP00000487317.1:n.*2184G=
NM_198892.1:c.3208G= (BMP2K)	NP_942595.1:p.Gly1070=
XM_005263117.1:c.3097G= (BMP2K)	XP_005263174.1:p.Gly1033=
XM_011532101.1:c.2968G= (BMP2K)	XP_011530403.1:p.Gly990=
XR_938694.1:n.1118-5594C= (PAQR3)
XM_017008381.1:c.2968G= (BMP2K)	XP_016863870.1:p.Gly990=
XM_017008382.1:c.2320G= (BMP2K)	XP_016863871.1:p.Gly774=
XR_938694.3:n.1098-5594C= (PAQR3)
NM_198892.2:c.3208G= (BMP2K) MANE Select	NP_942595.1:p.Gly1070=