Canonical Allele Identifier: CA357404871

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832982A>T (hg19) ; chr4:g.78911828A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911828A>T , CM000666.2:g.78911828A>T	GRCh38
NC_000004.11:g.79832982A>T , CM000666.1:g.79832982A>T	GRCh37
NC_000004.10:g.80052006A>T	NCBI36
NG_047162.1:g.140451A>T
NG_053104.1:g.32611T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3281A>T (BMP2K) MANE Select	ENSP00000424668.2:p.Asp1094Val
ENST00000335016.9:c.3281A>T (BMP2K)	ENSP00000334836.5:p.Asp1094Val
ENST00000342820.10:c.*782+3382T>A (PAQR3)	ENSP00000344203.6:n.*782+3382T>A
ENST00000502613.1:c.2358A>T (BMP2K)
ENST00000511594.5:c.*361T>A (PAQR3)	ENSP00000425080.1:n.*361T>A
ENST00000512760.5:c.*792+3382T>A (PAQR3)	ENSP00000426875.1:n.*792+3382T>A
ENST00000628286.1:c.*2257A>T (BMP2K)	ENSP00000487317.1:n.*2257A>T
NM_198892.1:c.3281A>T (BMP2K)	NP_942595.1:p.Asp1094Val
XM_005263117.1:c.3170A>T (BMP2K)	XP_005263174.1:p.Asp1057Val
XM_011532101.1:c.3041A>T (BMP2K)	XP_011530403.1:p.Asp1014Val
XR_938694.1:n.1118-5667T>A (PAQR3)
XM_017008381.1:c.3041A>T (BMP2K)	XP_016863870.1:p.Asp1014Val
XM_017008382.1:c.2393A>T (BMP2K)	XP_016863871.1:p.Asp798Val
XR_938694.3:n.1098-5667T>A (PAQR3)
NM_198892.2:c.3281A>T (BMP2K) MANE Select	NP_942595.1:p.Asp1094Val