Canonical Allele Identifier: CA1321544785
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530579_202530583delinsTTTAG , CM000664.2:g.202530579_202530583delinsTTTAG GRCh38
NC_000002.11:g.203395302_203395306delinsTTTAG , CM000664.1:g.203395302_203395306delinsTTTAG GRCh37
NC_000002.10:g.203103547_203103551delinsTTTAG NCBI36
NG_009363.1:g.159253_159257delinsTTTAG , LRG_712:g.159253_159257delinsTTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-215_968-211delinsTTTAG MANE Select ENSP00000363708.4:n.968-215_968-211delinsTTTAG
ENST00000638587.1:c.899-215_899-211delinsTTTAG ENSP00000491062.1:n.899-215_899-211delinsTTTAG
ENST00000374574.2:c.968-215_968-211delinsTTTAG ENSP00000363702.2:n.968-215_968-211delinsTTTAG
ENST00000374580.8:c.968-215_968-211delinsTTTAG ENSP00000363708.4:n.968-215_968-211delinsTTTAG
NM_001204.6:c.968-215_968-211delinsTTTAG , LRG_712t1:c.968-215_968-211delinsTTTAG NP_001195.2:n.968-215_968-211delinsTTTAG
XM_011511687.1:c.968-215_968-211delinsTTTAG XP_011509989.1:n.968-215_968-211delinsTTTAG
XM_011511688.1:c.968-215_968-211delinsTTTAG XP_011509990.1:n.968-215_968-211delinsTTTAG
NM_001204.7:c.968-215_968-211delinsTTTAG MANE Select NP_001195.2:n.968-215_968-211delinsTTTAG
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