Canonical Allele Identifier: CA440225896

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832572G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911418G>C , CM000666.2:g.78911418G>C	GRCh38
NC_000004.11:g.79832572G>C , CM000666.1:g.79832572G>C	GRCh37
NC_000004.10:g.80051596G>C	NCBI36
NG_047162.1:g.140041G>C
NG_053104.1:g.33021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2871G>C (BMP2K) MANE Select	ENSP00000424668.2:p.Val957=
ENST00000335016.9:c.2871G>C (BMP2K)	ENSP00000334836.5:p.Val957=
ENST00000342820.10:c.*782+3792C>G (PAQR3)	ENSP00000344203.6:n.*782+3792C>G
ENST00000502613.1:c.1948G>C (BMP2K)
ENST00000511594.5:c.*771C>G (PAQR3)	ENSP00000425080.1:n.*771C>G
ENST00000512760.5:c.*792+3792C>G (PAQR3)	ENSP00000426875.1:n.*792+3792C>G
ENST00000628286.1:c.*1847G>C (BMP2K)	ENSP00000487317.1:n.*1847G>C
NM_198892.1:c.2871G>C (BMP2K)	NP_942595.1:p.Val957=
XM_005263117.1:c.2760G>C (BMP2K)	XP_005263174.1:p.Val920=
XM_011532101.1:c.2631G>C (BMP2K)	XP_011530403.1:p.Val877=
XR_938694.1:n.1118-5257C>G (PAQR3)
XM_017008381.1:c.2631G>C (BMP2K)	XP_016863870.1:p.Val877=
XM_017008382.1:c.1983G>C (BMP2K)	XP_016863871.1:p.Val661=
XR_938694.3:n.1098-5257C>G (PAQR3)
NM_198892.2:c.2871G>C (BMP2K) MANE Select	NP_942595.1:p.Val957=