Canonical Allele Identifier: CA357404547

Gene: BMP2K PAQR3

Linked Data

• MyVariant Identifiers: chr4:g.79832831A>T (hg19) ; chr4:g.78911677A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911677A>T , CM000666.2:g.78911677A>T	GRCh38
NC_000004.11:g.79832831A>T , CM000666.1:g.79832831A>T	GRCh37
NC_000004.10:g.80051855A>T	NCBI36
NG_047162.1:g.140300A>T
NG_053104.1:g.32762T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3130A>T (BMP2K) MANE Select	ENSP00000424668.2:p.Asn1044Tyr
ENST00000335016.9:c.3130A>T (BMP2K)	ENSP00000334836.5:p.Asn1044Tyr
ENST00000342820.10:c.*782+3533T>A (PAQR3)	ENSP00000344203.6:n.*782+3533T>A
ENST00000502613.1:c.2207A>T (BMP2K)
ENST00000511594.5:c.*512T>A (PAQR3)	ENSP00000425080.1:n.*512T>A
ENST00000512760.5:c.*792+3533T>A (PAQR3)	ENSP00000426875.1:n.*792+3533T>A
ENST00000628286.1:c.*2106A>T (BMP2K)	ENSP00000487317.1:n.*2106A>T
NM_198892.1:c.3130A>T (BMP2K)	NP_942595.1:p.Asn1044Tyr
XM_005263117.1:c.3019A>T (BMP2K)	XP_005263174.1:p.Asn1007Tyr
XM_011532101.1:c.2890A>T (BMP2K)	XP_011530403.1:p.Asn964Tyr
XR_938694.1:n.1118-5516T>A (PAQR3)
XM_017008381.1:c.2890A>T (BMP2K)	XP_016863870.1:p.Asn964Tyr
XM_017008382.1:c.2242A>T (BMP2K)	XP_016863871.1:p.Asn748Tyr
XR_938694.3:n.1098-5516T>A (PAQR3)
NM_198892.2:c.3130A>T (BMP2K) MANE Select	NP_942595.1:p.Asn1044Tyr