Canonical Allele Identifier: CA1470756888

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911862A= , CM000666.2:g.78911862A= GRCh38
NC_000004.11:g.79833016A= , CM000666.1:g.79833016A= GRCh37
NC_000004.10:g.80052040A= NCBI36
NG_047162.1:g.140485A=
NG_053104.1:g.32577T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3315A= (BMP2K) MANE Select ENSP00000424668.2:p.Gln1105=
ENST00000335016.9:c.3315A= (BMP2K) ENSP00000334836.5:p.Gln1105=
ENST00000342820.10:c.*782+3348T= (PAQR3) ENSP00000344203.6:n.*782+3348T=
ENST00000502613.1:c.2392A= (BMP2K)
ENST00000511594.5:c.*327T= (PAQR3) ENSP00000425080.1:n.*327T=
ENST00000512760.5:c.*792+3348T= (PAQR3) ENSP00000426875.1:n.*792+3348T=
ENST00000628286.1:c.*2291A= (BMP2K) ENSP00000487317.1:n.*2291A=
NM_198892.1:c.3315A= (BMP2K) NP_942595.1:p.Gln1105=
XM_005263117.1:c.3204A= (BMP2K) XP_005263174.1:p.Gln1068=
XM_011532101.1:c.3075A= (BMP2K) XP_011530403.1:p.Gln1025=
XR_938694.1:n.1118-5701T= (PAQR3)
XM_017008381.1:c.3075A= (BMP2K) XP_016863870.1:p.Gln1025=
XM_017008382.1:c.2427A= (BMP2K) XP_016863871.1:p.Gln809=
XR_938694.3:n.1098-5701T= (PAQR3)
NM_198892.2:c.3315A= (BMP2K) MANE Select NP_942595.1:p.Gln1105=