Canonical Allele Identifier: CA1041346368
Gene: BMPR2 HGNC NCBI

Linked Data

gnomAD v3: 2-202530604-C-CGTTAATGTTT
gnomAD v4: 2-202530604-C-CGTTAATGTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530604_202530605insGTTAATGTTT , CM000664.2:g.202530604_202530605insGTTAATGTTT GRCh38
NC_000002.11:g.203395327_203395328insGTTAATGTTT , CM000664.1:g.203395327_203395328insGTTAATGTTT GRCh37
NC_000002.10:g.203103572_203103573insGTTAATGTTT NCBI36
NG_009363.1:g.159278_159279insGTTAATGTTT , LRG_712:g.159278_159279insGTTAATGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-190_968-189insGTTAATGTTT MANE Select ENSP00000363708.4:n.968-190_968-189insGTTAATGTTT
ENST00000638587.1:c.899-190_899-189insGTTAATGTTT ENSP00000491062.1:n.899-190_899-189insGTTAATGTTT
ENST00000374574.2:c.968-190_968-189insGTTAATGTTT ENSP00000363702.2:n.968-190_968-189insGTTAATGTTT
ENST00000374580.8:c.968-190_968-189insGTTAATGTTT ENSP00000363708.4:n.968-190_968-189insGTTAATGTTT
NM_001204.6:c.968-190_968-189insGTTAATGTTT , LRG_712t1:c.968-190_968-189insGTTAATGTTT NP_001195.2:n.968-190_968-189insGTTAATGTTT
XM_011511687.1:c.968-190_968-189insGTTAATGTTT XP_011509989.1:n.968-190_968-189insGTTAATGTTT
XM_011511688.1:c.968-190_968-189insGTTAATGTTT XP_011509990.1:n.968-190_968-189insGTTAATGTTT
NM_001204.7:c.968-190_968-189insGTTAATGTTT MANE Select NP_001195.2:n.968-190_968-189insGTTAATGTTT
Search 100 bp 5'
Search 100 bp 3'