Canonical Allele Identifier: CA1321559884
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556231_202556232delinsAC , CM000664.2:g.202556231_202556232delinsAC GRCh38
NC_000002.11:g.203420954_203420955delinsAC , CM000664.1:g.203420954_203420955delinsAC GRCh37
NC_000002.10:g.203129199_203129200delinsAC NCBI36
NG_009363.1:g.184905_184906delinsAC , LRG_712:g.184905_184906delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2566_2567delinsAC MANE Select ENSP00000363708.4:p.Thr856=
ENST00000638587.1:c.2497_2498delinsAC ENSP00000491062.1:n.2497_2498delinsAC
ENST00000374574.2:c.1586+3343_1586+3344delinsAC ENSP00000363702.2:n.1586+3343_1586+3344delinsAC
ENST00000374580.8:c.2566_2567delinsAC ENSP00000363708.4:p.Thr856=
NM_001204.6:c.2566_2567delinsAC , LRG_712t1:c.2566_2567delinsAC NP_001195.2:p.Thr856=
XM_011511687.1:c.2566_2567delinsAC XP_011509989.1:p.Thr856=
XM_011511688.1:c.1586+3343_1586+3344delinsAC XP_011509990.1:n.1586+3343_1586+3344delinsAC
NM_001204.7:c.2566_2567delinsAC MANE Select NP_001195.2:p.Thr856=