Canonical Allele Identifier: CA1321559938
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556271_202556272delinsCT , CM000664.2:g.202556271_202556272delinsCT GRCh38
NC_000002.11:g.203420994_203420995delinsCT , CM000664.1:g.203420994_203420995delinsCT GRCh37
NC_000002.10:g.203129239_203129240delinsCT NCBI36
NG_009363.1:g.184945_184946delinsCT , LRG_712:g.184945_184946delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2606_2607delinsCT MANE Select ENSP00000363708.4:p.Pro869=
ENST00000638587.1:c.2537_2538delinsCT ENSP00000491062.1:n.2537_2538delinsCT
ENST00000374574.2:c.1586+3383_1586+3384delinsCT ENSP00000363702.2:n.1586+3383_1586+3384delinsCT
ENST00000374580.8:c.2606_2607delinsCT ENSP00000363708.4:p.Pro869=
NM_001204.6:c.2606_2607delinsCT , LRG_712t1:c.2606_2607delinsCT NP_001195.2:p.Pro869=
XM_011511687.1:c.2606_2607delinsCT XP_011509989.1:p.Pro869=
XM_011511688.1:c.1586+3383_1586+3384delinsCT XP_011509990.1:n.1586+3383_1586+3384delinsCT
NM_001204.7:c.2606_2607delinsCT MANE Select NP_001195.2:p.Pro869=