Canonical Allele Identifier: CA440226402

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832497T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911343T>C , CM000666.2:g.78911343T>C	GRCh38
NC_000004.11:g.79832497T>C , CM000666.1:g.79832497T>C	GRCh37
NC_000004.10:g.80051521T>C	NCBI36
NG_047162.1:g.139966T>C
NG_053104.1:g.33096A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2796T>C (BMP2K) MANE Select	ENSP00000424668.2:p.Phe932=
ENST00000335016.9:c.2796T>C (BMP2K)	ENSP00000334836.5:p.Phe932=
ENST00000342820.10:c.*782+3867A>G (PAQR3)	ENSP00000344203.6:n.*782+3867A>G
ENST00000502613.1:c.1873T>C (BMP2K)
ENST00000511594.5:c.*846A>G (PAQR3)	ENSP00000425080.1:n.*846A>G
ENST00000512760.5:c.*792+3867A>G (PAQR3)	ENSP00000426875.1:n.*792+3867A>G
ENST00000628286.1:c.*1772T>C (BMP2K)	ENSP00000487317.1:n.*1772T>C
NM_198892.1:c.2796T>C (BMP2K)	NP_942595.1:p.Phe932=
XM_005263117.1:c.2685T>C (BMP2K)	XP_005263174.1:p.Phe895=
XM_011532101.1:c.2556T>C (BMP2K)	XP_011530403.1:p.Phe852=
XR_938694.1:n.1118-5182A>G (PAQR3)
XM_017008381.1:c.2556T>C (BMP2K)	XP_016863870.1:p.Phe852=
XM_017008382.1:c.1908T>C (BMP2K)	XP_016863871.1:p.Phe636=
XR_938694.3:n.1098-5182A>G (PAQR3)
NM_198892.2:c.2796T>C (BMP2K) MANE Select	NP_942595.1:p.Phe932=