Canonical Allele Identifier: CA1470756650

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911327A= , CM000666.2:g.78911327A= GRCh38
NC_000004.11:g.79832481A= , CM000666.1:g.79832481A= GRCh37
NC_000004.10:g.80051505A= NCBI36
NG_047162.1:g.139950A=
NG_053104.1:g.33112T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2780A= (BMP2K) MANE Select ENSP00000424668.2:p.Lys927=
ENST00000335016.9:c.2780A= (BMP2K) ENSP00000334836.5:p.Lys927=
ENST00000342820.10:c.*782+3883T= (PAQR3) ENSP00000344203.6:n.*782+3883T=
ENST00000502613.1:c.1857A= (BMP2K)
ENST00000511594.5:c.*862T= (PAQR3) ENSP00000425080.1:n.*862T=
ENST00000512760.5:c.*792+3883T= (PAQR3) ENSP00000426875.1:n.*792+3883T=
ENST00000628286.1:c.*1756A= (BMP2K) ENSP00000487317.1:n.*1756A=
NM_198892.1:c.2780A= (BMP2K) NP_942595.1:p.Lys927=
XM_005263117.1:c.2669A= (BMP2K) XP_005263174.1:p.Lys890=
XM_011532101.1:c.2540A= (BMP2K) XP_011530403.1:p.Lys847=
XR_938694.1:n.1118-5166T= (PAQR3)
XM_017008381.1:c.2540A= (BMP2K) XP_016863870.1:p.Lys847=
XM_017008382.1:c.1892A= (BMP2K) XP_016863871.1:p.Lys631=
XR_938694.3:n.1098-5166T= (PAQR3)
NM_198892.2:c.2780A= (BMP2K) MANE Select NP_942595.1:p.Lys927=