Canonical Allele Identifier: CA1321544813
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530638_202530639delinsTA , CM000664.2:g.202530638_202530639delinsTA GRCh38
NC_000002.11:g.203395361_203395362delinsTA , CM000664.1:g.203395361_203395362delinsTA GRCh37
NC_000002.10:g.203103606_203103607delinsTA NCBI36
NG_009363.1:g.159312_159313delinsTA , LRG_712:g.159312_159313delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-156_968-155delinsTA MANE Select ENSP00000363708.4:n.968-156_968-155delinsTA
ENST00000638587.1:c.899-156_899-155delinsTA ENSP00000491062.1:n.899-156_899-155delinsTA
ENST00000374574.2:c.968-156_968-155delinsTA ENSP00000363702.2:n.968-156_968-155delinsTA
ENST00000374580.8:c.968-156_968-155delinsTA ENSP00000363708.4:n.968-156_968-155delinsTA
NM_001204.6:c.968-156_968-155delinsTA , LRG_712t1:c.968-156_968-155delinsTA NP_001195.2:n.968-156_968-155delinsTA
XM_011511687.1:c.968-156_968-155delinsTA XP_011509989.1:n.968-156_968-155delinsTA
XM_011511688.1:c.968-156_968-155delinsTA XP_011509990.1:n.968-156_968-155delinsTA
NM_001204.7:c.968-156_968-155delinsTA MANE Select NP_001195.2:n.968-156_968-155delinsTA
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