Canonical Allele Identifier: CA1470756695

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911425G= , CM000666.2:g.78911425G= GRCh38
NC_000004.11:g.79832579G= , CM000666.1:g.79832579G= GRCh37
NC_000004.10:g.80051603G= NCBI36
NG_047162.1:g.140048G=
NG_053104.1:g.33014C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2878G= (BMP2K) MANE Select ENSP00000424668.2:p.Asp960=
ENST00000335016.9:c.2878G= (BMP2K) ENSP00000334836.5:p.Asp960=
ENST00000342820.10:c.*782+3785C= (PAQR3) ENSP00000344203.6:n.*782+3785C=
ENST00000502613.1:c.1955G= (BMP2K)
ENST00000511594.5:c.*764C= (PAQR3) ENSP00000425080.1:n.*764C=
ENST00000512760.5:c.*792+3785C= (PAQR3) ENSP00000426875.1:n.*792+3785C=
ENST00000628286.1:c.*1854G= (BMP2K) ENSP00000487317.1:n.*1854G=
NM_198892.1:c.2878G= (BMP2K) NP_942595.1:p.Asp960=
XM_005263117.1:c.2767G= (BMP2K) XP_005263174.1:p.Asp923=
XM_011532101.1:c.2638G= (BMP2K) XP_011530403.1:p.Asp880=
XR_938694.1:n.1118-5264C= (PAQR3)
XM_017008381.1:c.2638G= (BMP2K) XP_016863870.1:p.Asp880=
XM_017008382.1:c.1990G= (BMP2K) XP_016863871.1:p.Asp664=
XR_938694.3:n.1098-5264C= (PAQR3)
NM_198892.2:c.2878G= (BMP2K) MANE Select NP_942595.1:p.Asp960=