Canonical Allele Identifier: CA1321559607
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556072_202556076delinsACAGT , CM000664.2:g.202556072_202556076delinsACAGT GRCh38
NC_000002.11:g.203420795_203420799delinsACAGT , CM000664.1:g.203420795_203420799delinsACAGT GRCh37
NC_000002.10:g.203129040_203129044delinsACAGT NCBI36
NG_009363.1:g.184746_184750delinsACAGT , LRG_712:g.184746_184750delinsACAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.2407_2411delinsACAGT MANE Select ENSP00000363708.4:p.Thr803=
ENST00000638587.1:c.2338_2342delinsACAGT ENSP00000491062.1:n.2338_2342delinsACAGT
ENST00000374574.2:c.1586+3184_1586+3188delinsACAGT ENSP00000363702.2:n.1586+3184_1586+3188de...
ENST00000374580.8:c.2407_2411delinsACAGT ENSP00000363708.4:p.Thr803=
NM_001204.6:c.2407_2411delinsACAGT , LRG_712t1:c.2407_2411delinsACAGT NP_001195.2:p.Thr803=
XM_011511687.1:c.2407_2411delinsACAGT XP_011509989.1:p.Thr803=
XM_011511688.1:c.1586+3184_1586+3188delinsACAGT XP_011509990.1:n.1586+3184_1586+3188delin...
NM_001204.7:c.2407_2411delinsACAGT MANE Select NP_001195.2:p.Thr803=