Canonical Allele Identifier: CA1321540396
Gene: BMPR2 HGNC NCBI
RPL13AP12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520600G= , CM000664.2:g.202520600G= GRCh38
NC_000002.11:g.203385323G= , CM000664.1:g.203385323G= GRCh37
NC_000002.10:g.203093568G= NCBI36
NG_009363.1:g.149274G= , LRG_712:g.149274G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.967+399G= (BMPR2) MANE Select ENSP00000363708.4:n.967+399G=
ENST00000638587.1:c.898+399G= (BMPR2) ENSP00000491062.1:n.898+399G=
ENST00000374574.2:c.967+399G= (BMPR2) ENSP00000363702.2:n.967+399G=
ENST00000374580.8:c.967+399G= (BMPR2) ENSP00000363708.4:n.967+399G=
ENST00000435125.1:n.200G= (RPL13AP12)
NM_001204.6:c.967+399G= , LRG_712t1:c.967+399G= (BMPR2) NP_001195.2:n.967+399G=
XM_011511687.1:c.967+399G= (BMPR2) XP_011509989.1:n.967+399G=
XM_011511688.1:c.967+399G= (BMPR2) XP_011509990.1:n.967+399G=
NM_001204.7:c.967+399G= (BMPR2) MANE Select NP_001195.2:n.967+399G=