Canonical Allele Identifier: CA357401734

Gene: BMP2K PAQR3

Linked Data

• COSMIC: COSM4789711
• MyVariant Identifiers: chr4:g.79832445T>A (hg19) ; chr4:g.78911291T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911291T>A , CM000666.2:g.78911291T>A	GRCh38
NC_000004.11:g.79832445T>A , CM000666.1:g.79832445T>A	GRCh37
NC_000004.10:g.80051469T>A	NCBI36
NG_047162.1:g.139914T>A
NG_053104.1:g.33148A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2744T>A (BMP2K) MANE Select	ENSP00000424668.2:p.Val915Glu
ENST00000335016.9:c.2744T>A (BMP2K)	ENSP00000334836.5:p.Val915Glu
ENST00000342820.10:c.*782+3919A>T (PAQR3)	ENSP00000344203.6:n.*782+3919A>T
ENST00000502613.1:c.1821T>A (BMP2K)
ENST00000511594.5:c.*898A>T (PAQR3)	ENSP00000425080.1:n.*898A>T
ENST00000512760.5:c.*792+3919A>T (PAQR3)	ENSP00000426875.1:n.*792+3919A>T
ENST00000628286.1:c.*1720T>A (BMP2K)	ENSP00000487317.1:n.*1720T>A
NM_198892.1:c.2744T>A (BMP2K)	NP_942595.1:p.Val915Glu
XM_005263117.1:c.2633T>A (BMP2K)	XP_005263174.1:p.Val878Glu
XM_011532101.1:c.2504T>A (BMP2K)	XP_011530403.1:p.Val835Glu
XR_938694.1:n.1118-5130A>T (PAQR3)
XM_017008381.1:c.2504T>A (BMP2K)	XP_016863870.1:p.Val835Glu
XM_017008382.1:c.1856T>A (BMP2K)	XP_016863871.1:p.Val619Glu
XR_938694.3:n.1098-5130A>T (PAQR3)
NM_198892.2:c.2744T>A (BMP2K) MANE Select	NP_942595.1:p.Val915Glu