Canonical Allele Identifier: CA357404634

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832873G>T (hg19) ; chr4:g.78911719G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911719G>T , CM000666.2:g.78911719G>T	GRCh38
NC_000004.11:g.79832873G>T , CM000666.1:g.79832873G>T	GRCh37
NC_000004.10:g.80051897G>T	NCBI36
NG_047162.1:g.140342G>T
NG_053104.1:g.32720C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3172G>T (BMP2K) MANE Select	ENSP00000424668.2:p.Val1058Phe
ENST00000335016.9:c.3172G>T (BMP2K)	ENSP00000334836.5:p.Val1058Phe
ENST00000342820.10:c.*782+3491C>A (PAQR3)	ENSP00000344203.6:n.*782+3491C>A
ENST00000502613.1:c.2249G>T (BMP2K)
ENST00000511594.5:c.*470C>A (PAQR3)	ENSP00000425080.1:n.*470C>A
ENST00000512760.5:c.*792+3491C>A (PAQR3)	ENSP00000426875.1:n.*792+3491C>A
ENST00000628286.1:c.*2148G>T (BMP2K)	ENSP00000487317.1:n.*2148G>T
NM_198892.1:c.3172G>T (BMP2K)	NP_942595.1:p.Val1058Phe
XM_005263117.1:c.3061G>T (BMP2K)	XP_005263174.1:p.Val1021Phe
XM_011532101.1:c.2932G>T (BMP2K)	XP_011530403.1:p.Val978Phe
XR_938694.1:n.1118-5558C>A (PAQR3)
XM_017008381.1:c.2932G>T (BMP2K)	XP_016863870.1:p.Val978Phe
XM_017008382.1:c.2284G>T (BMP2K)	XP_016863871.1:p.Val762Phe
XR_938694.3:n.1098-5558C>A (PAQR3)
NM_198892.2:c.3172G>T (BMP2K) MANE Select	NP_942595.1:p.Val1058Phe