Canonical Allele Identifier: CA2511687453
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556292_202556293insTTTCTTGGGCCCTATGTGTC , CM000664.2:g.202556292_202556293insTTTCTTGGGCCCTATGTGTC GRCh38
NC_000002.11:g.203421015_203421016insTTTCTTGGGCCCTATGTGTC , CM000664.1:g.203421015_203421016insTTTCTTGGGCCCTATGTGTC GRCh37
NC_000002.10:g.203129260_203129261insTTTCTTGGGCCCTATGTGTC NCBI36
NG_009363.1:g.184966_184967insTTTCTTGGGCCCTATGTGTC , LRG_712:g.184966_184967insTTTCTTGGGCCCTATGTGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.2627_2628insTTTCTTGGGCCCTATGTGTC MANE Select ENSP00000363708.4:p.Gln876HisfsTer27
ENST00000638587.1:c.2558_2559insTTTCTTGGGCCCTATGTGTC ENSP00000491062.1:n.2558_2559insTTTCTTGGG...
ENST00000374574.2:c.1587-3404_1587-3403insTTTCTTGGGCCCTATGTGTC ENSP00000363702.2:n.1587-3404_1587-3403in...
ENST00000374580.8:c.2627_2628insTTTCTTGGGCCCTATGTGTC ENSP00000363708.4:p.Gln876HisfsTer27
NM_001204.6:c.2627_2628insTTTCTTGGGCCCTATGTGTC , LRG_712t1:c.2627_2628insTTTCTTGGGCCCTATGTGTC NP_001195.2:p.Gln876HisfsTer27
XM_011511687.1:c.2627_2628insTTTCTTGGGCCCTATGTGTC XP_011509989.1:p.Gln876HisfsTer27
XM_011511688.1:c.1587-3404_1587-3403insTTTCTTGGGCCCTATGTGTC XP_011509990.1:n.1587-3404_1587-3403insTT...
NM_001204.7:c.2627_2628insTTTCTTGGGCCCTATGTGTC MANE Select NP_001195.2:p.Gln876HisfsTer27