Canonical Allele Identifier: CA357404751

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911773T>A , CM000666.2:g.78911773T>A GRCh38
NC_000004.11:g.79832927T>A , CM000666.1:g.79832927T>A GRCh37
NC_000004.10:g.80051951T>A NCBI36
NG_047162.1:g.140396T>A
NG_053104.1:g.32666A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3226T>A (BMP2K) MANE Select ENSP00000424668.2:p.Ser1076Thr
ENST00000335016.9:c.3226T>A (BMP2K) ENSP00000334836.5:p.Ser1076Thr
ENST00000342820.10:c.*782+3437A>T (PAQR3) ENSP00000344203.6:n.*782+3437A>T
ENST00000502613.1:c.2303T>A (BMP2K)
ENST00000511594.5:c.*416A>T (PAQR3) ENSP00000425080.1:n.*416A>T
ENST00000512760.5:c.*792+3437A>T (PAQR3) ENSP00000426875.1:n.*792+3437A>T
ENST00000628286.1:c.*2202T>A (BMP2K) ENSP00000487317.1:n.*2202T>A
NM_198892.1:c.3226T>A (BMP2K) NP_942595.1:p.Ser1076Thr
XM_005263117.1:c.3115T>A (BMP2K) XP_005263174.1:p.Ser1039Thr
XM_011532101.1:c.2986T>A (BMP2K) XP_011530403.1:p.Ser996Thr
XR_938694.1:n.1118-5612A>T (PAQR3)
XM_017008381.1:c.2986T>A (BMP2K) XP_016863870.1:p.Ser996Thr
XM_017008382.1:c.2338T>A (BMP2K) XP_016863871.1:p.Ser780Thr
XR_938694.3:n.1098-5612A>T (PAQR3)
NM_198892.2:c.3226T>A (BMP2K) MANE Select NP_942595.1:p.Ser1076Thr