Canonical Allele Identifier: CA1321544836
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530669_202530672delinsCTCT , CM000664.2:g.202530669_202530672delinsCTCT GRCh38
NC_000002.11:g.203395392_203395395delinsCTCT , CM000664.1:g.203395392_203395395delinsCTCT GRCh37
NC_000002.10:g.203103637_203103640delinsCTCT NCBI36
NG_009363.1:g.159343_159346delinsCTCT , LRG_712:g.159343_159346delinsCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-125_968-122delinsCTCT MANE Select ENSP00000363708.4:n.968-125_968-122delinsCTCT
ENST00000638587.1:c.899-125_899-122delinsCTCT ENSP00000491062.1:n.899-125_899-122delinsCTCT
ENST00000374574.2:c.968-125_968-122delinsCTCT ENSP00000363702.2:n.968-125_968-122delinsCTCT
ENST00000374580.8:c.968-125_968-122delinsCTCT ENSP00000363708.4:n.968-125_968-122delinsCTCT
NM_001204.6:c.968-125_968-122delinsCTCT , LRG_712t1:c.968-125_968-122delinsCTCT NP_001195.2:n.968-125_968-122delinsCTCT
XM_011511687.1:c.968-125_968-122delinsCTCT XP_011509989.1:n.968-125_968-122delinsCTCT
XM_011511688.1:c.968-125_968-122delinsCTCT XP_011509990.1:n.968-125_968-122delinsCTCT
NM_001204.7:c.968-125_968-122delinsCTCT MANE Select NP_001195.2:n.968-125_968-122delinsCTCT
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