Canonical Allele Identifier: CA1321559152
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202555736A= , CM000664.2:g.202555736A= GRCh38
NC_000002.11:g.203420459A= , CM000664.1:g.203420459A= GRCh37
NC_000002.10:g.203128704A= NCBI36
NG_009363.1:g.184410A= , LRG_712:g.184410A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2071A= MANE Select ENSP00000363708.4:p.Lys691=
ENST00000638587.1:c.2002A= ENSP00000491062.1:n.2002A=
ENST00000374574.2:c.1586+2848A= ENSP00000363702.2:n.1586+2848A=
ENST00000374580.8:c.2071A= ENSP00000363708.4:p.Lys691=
NM_001204.6:c.2071A= , LRG_712t1:c.2071A= NP_001195.2:p.Lys691=
XM_011511687.1:c.2071A= XP_011509989.1:p.Lys691=
XM_011511688.1:c.1586+2848A= XP_011509990.1:n.1586+2848A=
NM_001204.7:c.2071A= MANE Select NP_001195.2:p.Lys691=