Canonical Allele Identifier: CA357404457

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911659A>T , CM000666.2:g.78911659A>T GRCh38
NC_000004.11:g.79832813A>T , CM000666.1:g.79832813A>T GRCh37
NC_000004.10:g.80051837A>T NCBI36
NG_047162.1:g.140282A>T
NG_053104.1:g.32780T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3112A>T (BMP2K) MANE Select ENSP00000424668.2:p.Ile1038Phe
ENST00000335016.9:c.3112A>T (BMP2K) ENSP00000334836.5:p.Ile1038Phe
ENST00000342820.10:c.*782+3551T>A (PAQR3) ENSP00000344203.6:n.*782+3551T>A
ENST00000502613.1:c.2189A>T (BMP2K)
ENST00000511594.5:c.*530T>A (PAQR3) ENSP00000425080.1:n.*530T>A
ENST00000512760.5:c.*792+3551T>A (PAQR3) ENSP00000426875.1:n.*792+3551T>A
ENST00000628286.1:c.*2088A>T (BMP2K) ENSP00000487317.1:n.*2088A>T
NM_198892.1:c.3112A>T (BMP2K) NP_942595.1:p.Ile1038Phe
XM_005263117.1:c.3001A>T (BMP2K) XP_005263174.1:p.Ile1001Phe
XM_011532101.1:c.2872A>T (BMP2K) XP_011530403.1:p.Ile958Phe
XR_938694.1:n.1118-5498T>A (PAQR3)
XM_017008381.1:c.2872A>T (BMP2K) XP_016863870.1:p.Ile958Phe
XM_017008382.1:c.2224A>T (BMP2K) XP_016863871.1:p.Ile742Phe
XR_938694.3:n.1098-5498T>A (PAQR3)
NM_198892.2:c.3112A>T (BMP2K) MANE Select NP_942595.1:p.Ile1038Phe