Canonical Allele Identifier: CA1321510762
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467691_202467696delinsTAAGTA , CM000664.2:g.202467691_202467696delinsTAAGTA GRCh38
NC_000002.11:g.203332414_203332419delinsTAAGTA , CM000664.1:g.203332414_203332419delinsTAAGTA GRCh37
NC_000002.10:g.203040659_203040664delinsTAAGTA NCBI36
NG_009363.1:g.96365_96370delinsTAAGTA , LRG_712:g.96365_96370delinsTAAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.418+2_418+7delinsTAAGTA MANE Select ENSP00000363708.4:n.418+2_418+7delinsTAAGTA
ENST00000638587.1:c.349+2_349+7delinsTAAGTA ENSP00000491062.1:n.349+2_349+7delinsTAAGTA
ENST00000374574.2:c.418+2_418+7delinsTAAGTA ENSP00000363702.2:n.418+2_418+7delinsTAAGTA
ENST00000374580.8:c.418+2_418+7delinsTAAGTA ENSP00000363708.4:n.418+2_418+7delinsTAAGTA
ENST00000479069.1:n.325+2_325+7delinsTAAGTA
NM_001204.6:c.418+2_418+7delinsTAAGTA , LRG_712t1:c.418+2_418+7delinsTAAGTA NP_001195.2:n.418+2_418+7delinsTAAGTA
XM_011511687.1:c.418+2_418+7delinsTAAGTA XP_011509989.1:n.418+2_418+7delinsTAAGTA
XM_011511688.1:c.418+2_418+7delinsTAAGTA XP_011509990.1:n.418+2_418+7delinsTAAGTA
NM_001204.7:c.418+2_418+7delinsTAAGTA MANE Select NP_001195.2:n.418+2_418+7delinsTAAGTA