Canonical Allele Identifier: CA1321559935
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556270_202556275delinsCCTTTA , CM000664.2:g.202556270_202556275delinsCCTTTA GRCh38
NC_000002.11:g.203420993_203420998delinsCCTTTA , CM000664.1:g.203420993_203420998delinsCCTTTA GRCh37
NC_000002.10:g.203129238_203129243delinsCCTTTA NCBI36
NG_009363.1:g.184944_184949delinsCCTTTA , LRG_712:g.184944_184949delinsCCTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2605_2610delinsCCTTTA MANE Select ENSP00000363708.4:p.Pro869=
ENST00000638587.1:c.2536_2541delinsCCTTTA ENSP00000491062.1:n.2536_2541delinsCCTTTA
ENST00000374574.2:c.1586+3382_1586+3387delinsCCTTTA ENSP00000363702.2:n.1586+3382_1586+3387delinsCCTTTA
ENST00000374580.8:c.2605_2610delinsCCTTTA ENSP00000363708.4:p.Pro869=
NM_001204.6:c.2605_2610delinsCCTTTA , LRG_712t1:c.2605_2610delinsCCTTTA NP_001195.2:p.Pro869=
XM_011511687.1:c.2605_2610delinsCCTTTA XP_011509989.1:p.Pro869=
XM_011511688.1:c.1586+3382_1586+3387delinsCCTTTA XP_011509990.1:n.1586+3382_1586+3387delinsCCTTTA
NM_001204.7:c.2605_2610delinsCCTTTA MANE Select NP_001195.2:p.Pro869=