Canonical Allele Identifier: CA357403000

Gene: BMP2K PAQR3

Linked Data

• COSMIC: COSM5014437
• MyVariant Identifiers: chr4:g.79832610T>G (hg19) ; chr4:g.78911456T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911456T>G , CM000666.2:g.78911456T>G	GRCh38
NC_000004.11:g.79832610T>G , CM000666.1:g.79832610T>G	GRCh37
NC_000004.10:g.80051634T>G	NCBI36
NG_047162.1:g.140079T>G
NG_053104.1:g.32983A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2909T>G (BMP2K) MANE Select	ENSP00000424668.2:p.Val970Gly
ENST00000335016.9:c.2909T>G (BMP2K)	ENSP00000334836.5:p.Val970Gly
ENST00000342820.10:c.*782+3754A>C (PAQR3)	ENSP00000344203.6:n.*782+3754A>C
ENST00000502613.1:c.1986T>G (BMP2K)
ENST00000511594.5:c.*733A>C (PAQR3)	ENSP00000425080.1:n.*733A>C
ENST00000512760.5:c.*792+3754A>C (PAQR3)	ENSP00000426875.1:n.*792+3754A>C
ENST00000628286.1:c.*1885T>G (BMP2K)	ENSP00000487317.1:n.*1885T>G
NM_198892.1:c.2909T>G (BMP2K)	NP_942595.1:p.Val970Gly
XM_005263117.1:c.2798T>G (BMP2K)	XP_005263174.1:p.Val933Gly
XM_011532101.1:c.2669T>G (BMP2K)	XP_011530403.1:p.Val890Gly
XR_938694.1:n.1118-5295A>C (PAQR3)
XM_017008381.1:c.2669T>G (BMP2K)	XP_016863870.1:p.Val890Gly
XM_017008382.1:c.2021T>G (BMP2K)	XP_016863871.1:p.Val674Gly
XR_938694.3:n.1098-5295A>C (PAQR3)
NM_198892.2:c.2909T>G (BMP2K) MANE Select	NP_942595.1:p.Val970Gly