Canonical Allele Identifier: CA440226201

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832704A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911550A>T , CM000666.2:g.78911550A>T	GRCh38
NC_000004.11:g.79832704A>T , CM000666.1:g.79832704A>T	GRCh37
NC_000004.10:g.80051728A>T	NCBI36
NG_047162.1:g.140173A>T
NG_053104.1:g.32889T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3003A>T (BMP2K) MANE Select	ENSP00000424668.2:p.Pro1001=
ENST00000335016.9:c.3003A>T (BMP2K)	ENSP00000334836.5:p.Pro1001=
ENST00000342820.10:c.*782+3660T>A (PAQR3)	ENSP00000344203.6:n.*782+3660T>A
ENST00000502613.1:c.2080A>T (BMP2K)
ENST00000511594.5:c.*639T>A (PAQR3)	ENSP00000425080.1:n.*639T>A
ENST00000512760.5:c.*792+3660T>A (PAQR3)	ENSP00000426875.1:n.*792+3660T>A
ENST00000628286.1:c.*1979A>T (BMP2K)	ENSP00000487317.1:n.*1979A>T
NM_198892.1:c.3003A>T (BMP2K)	NP_942595.1:p.Pro1001=
XM_005263117.1:c.2892A>T (BMP2K)	XP_005263174.1:p.Pro964=
XM_011532101.1:c.2763A>T (BMP2K)	XP_011530403.1:p.Pro921=
XR_938694.1:n.1118-5389T>A (PAQR3)
XM_017008381.1:c.2763A>T (BMP2K)	XP_016863870.1:p.Pro921=
XM_017008382.1:c.2115A>T (BMP2K)	XP_016863871.1:p.Pro705=
XR_938694.3:n.1098-5389T>A (PAQR3)
NM_198892.2:c.3003A>T (BMP2K) MANE Select	NP_942595.1:p.Pro1001=