Canonical Allele Identifier: CA357404720

Gene: BMP2K PAQR3

Linked Data

• dbSNP Id: rs1560561281
• gnomAD v4: 4-78911758-G-C
• MyVariant Identifiers: chr4:g.79832912G>C (hg19) ; chr4:g.78911758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911758G>C , CM000666.2:g.78911758G>C	GRCh38
NC_000004.11:g.79832912G>C , CM000666.1:g.79832912G>C	GRCh37
NC_000004.10:g.80051936G>C	NCBI36
NG_047162.1:g.140381G>C
NG_053104.1:g.32681C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3211G>C (BMP2K) MANE Select	ENSP00000424668.2:p.Ala1071Pro
ENST00000335016.9:c.3211G>C (BMP2K)	ENSP00000334836.5:p.Ala1071Pro
ENST00000342820.10:c.*782+3452C>G (PAQR3)	ENSP00000344203.6:n.*782+3452C>G
ENST00000502613.1:c.2288G>C (BMP2K)
ENST00000511594.5:c.*431C>G (PAQR3)	ENSP00000425080.1:n.*431C>G
ENST00000512760.5:c.*792+3452C>G (PAQR3)	ENSP00000426875.1:n.*792+3452C>G
ENST00000628286.1:c.*2187G>C (BMP2K)	ENSP00000487317.1:n.*2187G>C
NM_198892.1:c.3211G>C (BMP2K)	NP_942595.1:p.Ala1071Pro
XM_005263117.1:c.3100G>C (BMP2K)	XP_005263174.1:p.Ala1034Pro
XM_011532101.1:c.2971G>C (BMP2K)	XP_011530403.1:p.Ala991Pro
XR_938694.1:n.1118-5597C>G (PAQR3)
XM_017008381.1:c.2971G>C (BMP2K)	XP_016863870.1:p.Ala991Pro
XM_017008382.1:c.2323G>C (BMP2K)	XP_016863871.1:p.Ala775Pro
XR_938694.3:n.1098-5597C>G (PAQR3)
NM_198892.2:c.3211G>C (BMP2K) MANE Select	NP_942595.1:p.Ala1071Pro