Canonical Allele Identifier: CA440226270

Gene: BMP2K PAQR3

Linked Data

• gnomAD v4: 4-78911691-A-G
• MyVariant Identifiers: chr4:g.79832845A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911691A>G , CM000666.2:g.78911691A>G	GRCh38
NC_000004.11:g.79832845A>G , CM000666.1:g.79832845A>G	GRCh37
NC_000004.10:g.80051869A>G	NCBI36
NG_047162.1:g.140314A>G
NG_053104.1:g.32748T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3144A>G (BMP2K) MANE Select	ENSP00000424668.2:p.Ala1048=
ENST00000335016.9:c.3144A>G (BMP2K)	ENSP00000334836.5:p.Ala1048=
ENST00000342820.10:c.*782+3519T>C (PAQR3)	ENSP00000344203.6:n.*782+3519T>C
ENST00000502613.1:c.2221A>G (BMP2K)
ENST00000511594.5:c.*498T>C (PAQR3)	ENSP00000425080.1:n.*498T>C
ENST00000512760.5:c.*792+3519T>C (PAQR3)	ENSP00000426875.1:n.*792+3519T>C
ENST00000628286.1:c.*2120A>G (BMP2K)	ENSP00000487317.1:n.*2120A>G
NM_198892.1:c.3144A>G (BMP2K)	NP_942595.1:p.Ala1048=
XM_005263117.1:c.3033A>G (BMP2K)	XP_005263174.1:p.Ala1011=
XM_011532101.1:c.2904A>G (BMP2K)	XP_011530403.1:p.Ala968=
XR_938694.1:n.1118-5530T>C (PAQR3)
XM_017008381.1:c.2904A>G (BMP2K)	XP_016863870.1:p.Ala968=
XM_017008382.1:c.2256A>G (BMP2K)	XP_016863871.1:p.Ala752=
XR_938694.3:n.1098-5530T>C (PAQR3)
NM_198892.2:c.3144A>G (BMP2K) MANE Select	NP_942595.1:p.Ala1048=