Canonical Allele Identifier: CA440226498

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832980T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911826T>G , CM000666.2:g.78911826T>G	GRCh38
NC_000004.11:g.79832980T>G , CM000666.1:g.79832980T>G	GRCh37
NC_000004.10:g.80052004T>G	NCBI36
NG_047162.1:g.140449T>G
NG_053104.1:g.32613A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3279T>G (BMP2K) MANE Select	ENSP00000424668.2:p.Ala1093=
ENST00000335016.9:c.3279T>G (BMP2K)	ENSP00000334836.5:p.Ala1093=
ENST00000342820.10:c.*782+3384A>C (PAQR3)	ENSP00000344203.6:n.*782+3384A>C
ENST00000502613.1:c.2356T>G (BMP2K)
ENST00000511594.5:c.*363A>C (PAQR3)	ENSP00000425080.1:n.*363A>C
ENST00000512760.5:c.*792+3384A>C (PAQR3)	ENSP00000426875.1:n.*792+3384A>C
ENST00000628286.1:c.*2255T>G (BMP2K)	ENSP00000487317.1:n.*2255T>G
NM_198892.1:c.3279T>G (BMP2K)	NP_942595.1:p.Ala1093=
XM_005263117.1:c.3168T>G (BMP2K)	XP_005263174.1:p.Ala1056=
XM_011532101.1:c.3039T>G (BMP2K)	XP_011530403.1:p.Ala1013=
XR_938694.1:n.1118-5665A>C (PAQR3)
XM_017008381.1:c.3039T>G (BMP2K)	XP_016863870.1:p.Ala1013=
XM_017008382.1:c.2391T>G (BMP2K)	XP_016863871.1:p.Ala797=
XR_938694.3:n.1098-5665A>C (PAQR3)
NM_198892.2:c.3279T>G (BMP2K) MANE Select	NP_942595.1:p.Ala1093=