Canonical Allele Identifier: CA1321539662
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202518863_202518865delinsCTT , CM000664.2:g.202518863_202518865delinsCTT GRCh38
NC_000002.11:g.203383586_203383588delinsCTT , CM000664.1:g.203383586_203383588delinsCTT GRCh37
NC_000002.10:g.203091831_203091833delinsCTT NCBI36
NG_009363.1:g.147537_147539delinsCTT , LRG_712:g.147537_147539delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.663_665delinsCTT MANE Select ENSP00000363708.4:p.Ser221=
ENST00000638587.1:c.594_596delinsCTT ENSP00000491062.1:p.Ser198=
ENST00000374574.2:c.663_665delinsCTT ENSP00000363702.2:p.Ser221=
ENST00000374580.8:c.663_665delinsCTT ENSP00000363708.4:p.Ser221=
NM_001204.6:c.663_665delinsCTT , LRG_712t1:c.663_665delinsCTT NP_001195.2:p.Ser221=
XM_011511687.1:c.663_665delinsCTT XP_011509989.1:p.Ser221=
XM_011511688.1:c.663_665delinsCTT XP_011509990.1:p.Ser221=
NM_001204.7:c.663_665delinsCTT MANE Select NP_001195.2:p.Ser221=