Canonical Allele Identifier: CA2980640

Linked Data

dbSNP Id: rs779465739
gnomAD v2: 4-79832562-T-A
gnomAD v4: 4-78911408-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911408T>A , CM000666.2:g.78911408T>A GRCh38
NC_000004.11:g.79832562T>A , CM000666.1:g.79832562T>A GRCh37
NC_000004.10:g.80051586T>A NCBI36
NG_047162.1:g.140031T>A
NG_053104.1:g.33031A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2861T>A (BMP2K) MANE Select ENSP00000424668.2:p.Phe954Tyr
ENST00000335016.9:c.2861T>A (BMP2K) ENSP00000334836.5:p.Phe954Tyr
ENST00000342820.10:c.*782+3802A>T (PAQR3) ENSP00000344203.6:n.*782+3802A>T
ENST00000502613.1:c.1938T>A (BMP2K)
ENST00000511594.5:c.*781A>T (PAQR3) ENSP00000425080.1:n.*781A>T
ENST00000512760.5:c.*792+3802A>T (PAQR3) ENSP00000426875.1:n.*792+3802A>T
ENST00000628286.1:c.*1837T>A (BMP2K) ENSP00000487317.1:n.*1837T>A
NM_198892.1:c.2861T>A (BMP2K) NP_942595.1:p.Phe954Tyr
XM_005263117.1:c.2750T>A (BMP2K) XP_005263174.1:p.Phe917Tyr
XM_011532101.1:c.2621T>A (BMP2K) XP_011530403.1:p.Phe874Tyr
XR_938694.1:n.1118-5247A>T (PAQR3)
XM_017008381.1:c.2621T>A (BMP2K) XP_016863870.1:p.Phe874Tyr
XM_017008382.1:c.1973T>A (BMP2K) XP_016863871.1:p.Phe658Tyr
XR_938694.3:n.1098-5247A>T (PAQR3)
NM_198892.2:c.2861T>A (BMP2K) MANE Select NP_942595.1:p.Phe954Tyr