Canonical Allele Identifier: CA1470756645

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911315C= , CM000666.2:g.78911315C=	GRCh38
NC_000004.11:g.79832469C= , CM000666.1:g.79832469C=	GRCh37
NC_000004.10:g.80051493C=	NCBI36
NG_047162.1:g.139938C=
NG_053104.1:g.33124G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2768C= (BMP2K) MANE Select	ENSP00000424668.2:p.Pro923=
ENST00000335016.9:c.2768C= (BMP2K)	ENSP00000334836.5:p.Pro923=
ENST00000342820.10:c.*782+3895G= (PAQR3)	ENSP00000344203.6:n.*782+3895G=
ENST00000502613.1:c.1845C= (BMP2K)
ENST00000511594.5:c.*874G= (PAQR3)	ENSP00000425080.1:n.*874G=
ENST00000512760.5:c.*792+3895G= (PAQR3)	ENSP00000426875.1:n.*792+3895G=
ENST00000628286.1:c.*1744C= (BMP2K)	ENSP00000487317.1:n.*1744C=
NM_198892.1:c.2768C= (BMP2K)	NP_942595.1:p.Pro923=
XM_005263117.1:c.2657C= (BMP2K)	XP_005263174.1:p.Pro886=
XM_011532101.1:c.2528C= (BMP2K)	XP_011530403.1:p.Pro843=
XR_938694.1:n.1118-5154G= (PAQR3)
XM_017008381.1:c.2528C= (BMP2K)	XP_016863870.1:p.Pro843=
XM_017008382.1:c.1880C= (BMP2K)	XP_016863871.1:p.Pro627=
XR_938694.3:n.1098-5154G= (PAQR3)
NM_198892.2:c.2768C= (BMP2K) MANE Select	NP_942595.1:p.Pro923=