Canonical Allele Identifier: CA658761122
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202532703_202532704insGA , CM000664.2:g.202532703_202532704insGA GRCh38
NC_000002.11:g.203397426_203397427insGA , CM000664.1:g.203397426_203397427insGA GRCh37
NC_000002.10:g.203105671_203105672insGA NCBI36
NG_009363.1:g.161377_161378insGA , LRG_712:g.161377_161378insGA

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1247_1248insGA MANE Select ENSP00000363708.4:p.Ile416MetfsTer4
ENST00000638587.1:c.1178_1179insGA ENSP00000491062.1:p.Ile393MetfsTer4
ENST00000374574.2:c.1247_1248insGA ENSP00000363702.2:p.Ile416MetfsTer4
ENST00000374580.8:c.1247_1248insGA ENSP00000363708.4:p.Ile416MetfsTer4
NM_001204.6:c.1247_1248insGA , LRG_712t1:c.1247_1248insGA NP_001195.2:p.Ile416MetfsTer4
XM_011511687.1:c.1247_1248insGA XP_011509989.1:p.Ile416MetfsTer4
XM_011511688.1:c.1247_1248insGA XP_011509990.1:p.Ile416MetfsTer4
NM_001204.7:c.1247_1248insGA MANE Select NP_001195.2:p.Ile416MetfsTer4