Canonical Allele Identifier: CA440226121

Gene: BMP2K PAQR3

Linked Data

• dbSNP Id: rs1734605530
• gnomAD v4: 4-78911511-T-C
• MyVariant Identifiers: chr4:g.79832665T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911511T>C , CM000666.2:g.78911511T>C	GRCh38
NC_000004.11:g.79832665T>C , CM000666.1:g.79832665T>C	GRCh37
NC_000004.10:g.80051689T>C	NCBI36
NG_047162.1:g.140134T>C
NG_053104.1:g.32928A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2964T>C (BMP2K) MANE Select	ENSP00000424668.2:p.Asp988=
ENST00000335016.9:c.2964T>C (BMP2K)	ENSP00000334836.5:p.Asp988=
ENST00000342820.10:c.*782+3699A>G (PAQR3)	ENSP00000344203.6:n.*782+3699A>G
ENST00000502613.1:c.2041T>C (BMP2K)
ENST00000511594.5:c.*678A>G (PAQR3)	ENSP00000425080.1:n.*678A>G
ENST00000512760.5:c.*792+3699A>G (PAQR3)	ENSP00000426875.1:n.*792+3699A>G
ENST00000628286.1:c.*1940T>C (BMP2K)	ENSP00000487317.1:n.*1940T>C
NM_198892.1:c.2964T>C (BMP2K)	NP_942595.1:p.Asp988=
XM_005263117.1:c.2853T>C (BMP2K)	XP_005263174.1:p.Asp951=
XM_011532101.1:c.2724T>C (BMP2K)	XP_011530403.1:p.Asp908=
XR_938694.1:n.1118-5350A>G (PAQR3)
XM_017008381.1:c.2724T>C (BMP2K)	XP_016863870.1:p.Asp908=
XM_017008382.1:c.2076T>C (BMP2K)	XP_016863871.1:p.Asp692=
XR_938694.3:n.1098-5350A>G (PAQR3)
NM_198892.2:c.2964T>C (BMP2K) MANE Select	NP_942595.1:p.Asp988=