Canonical Allele Identifier: CA357403593

Gene: BMP2K PAQR3

Linked Data

• gnomAD v4: 4-78911542-G-T
• MyVariant Identifiers: chr4:g.79832696G>T (hg19) ; chr4:g.78911542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911542G>T , CM000666.2:g.78911542G>T	GRCh38
NC_000004.11:g.79832696G>T , CM000666.1:g.79832696G>T	GRCh37
NC_000004.10:g.80051720G>T	NCBI36
NG_047162.1:g.140165G>T
NG_053104.1:g.32897C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2995G>T (BMP2K) MANE Select	ENSP00000424668.2:p.Gly999Cys
ENST00000335016.9:c.2995G>T (BMP2K)	ENSP00000334836.5:p.Gly999Cys
ENST00000342820.10:c.*782+3668C>A (PAQR3)	ENSP00000344203.6:n.*782+3668C>A
ENST00000502613.1:c.2072G>T (BMP2K)
ENST00000511594.5:c.*647C>A (PAQR3)	ENSP00000425080.1:n.*647C>A
ENST00000512760.5:c.*792+3668C>A (PAQR3)	ENSP00000426875.1:n.*792+3668C>A
ENST00000628286.1:c.*1971G>T (BMP2K)	ENSP00000487317.1:n.*1971G>T
NM_198892.1:c.2995G>T (BMP2K)	NP_942595.1:p.Gly999Cys
XM_005263117.1:c.2884G>T (BMP2K)	XP_005263174.1:p.Gly962Cys
XM_011532101.1:c.2755G>T (BMP2K)	XP_011530403.1:p.Gly919Cys
XR_938694.1:n.1118-5381C>A (PAQR3)
XM_017008381.1:c.2755G>T (BMP2K)	XP_016863870.1:p.Gly919Cys
XM_017008382.1:c.2107G>T (BMP2K)	XP_016863871.1:p.Gly703Cys
XR_938694.3:n.1098-5381C>A (PAQR3)
NM_198892.2:c.2995G>T (BMP2K) MANE Select	NP_942595.1:p.Gly999Cys