Canonical Allele Identifier: CA1321540301
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520288_202520293delinsATAATT , CM000664.2:g.202520288_202520293delinsATAATT GRCh38
NC_000002.11:g.203385011_203385016delinsATAATT , CM000664.1:g.203385011_203385016delinsATAATT GRCh37
NC_000002.10:g.203093256_203093261delinsATAATT NCBI36
NG_009363.1:g.148962_148967delinsATAATT , LRG_712:g.148962_148967delinsATAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.967+87_967+92delinsATAATT MANE Select ENSP00000363708.4:n.967+87_967+92delinsATAATT
ENST00000638587.1:c.898+87_898+92delinsATAATT ENSP00000491062.1:n.898+87_898+92delinsATAATT
ENST00000374574.2:c.967+87_967+92delinsATAATT ENSP00000363702.2:n.967+87_967+92delinsATAATT
ENST00000374580.8:c.967+87_967+92delinsATAATT ENSP00000363708.4:n.967+87_967+92delinsATAATT
NM_001204.6:c.967+87_967+92delinsATAATT , LRG_712t1:c.967+87_967+92delinsATAATT NP_001195.2:n.967+87_967+92delinsATAATT
XM_011511687.1:c.967+87_967+92delinsATAATT XP_011509989.1:n.967+87_967+92delinsATAATT
XM_011511688.1:c.967+87_967+92delinsATAATT XP_011509990.1:n.967+87_967+92delinsATAATT
NM_001204.7:c.967+87_967+92delinsATAATT MANE Select NP_001195.2:n.967+87_967+92delinsATAATT