Canonical Allele Identifier: CA2662706486
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202542528_202542532dup , CM000664.2:g.202542528_202542532dup GRCh38
NC_000002.11:g.203407251_203407255dup , CM000664.1:g.203407251_203407255dup GRCh37
NC_000002.10:g.203115496_203115500dup NCBI36
NG_009363.1:g.171202_171206dup , LRG_712:g.171202_171206dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1413+81_1413+85dup MANE Select ENSP00000363708.4:n.1413+81_1413+85dup
ENST00000638587.1:c.1344+81_1344+85dup ENSP00000491062.1:n.1344+81_1344+85dup
ENST00000374574.2:c.1413+81_1413+85dup ENSP00000363702.2:n.1413+81_1413+85dup
ENST00000374580.8:c.1413+81_1413+85dup ENSP00000363708.4:n.1413+81_1413+85dup
NM_001204.6:c.1413+81_1413+85dup , LRG_712t1:c.1413+81_1413+85dup NP_001195.2:n.1413+81_1413+85dup
XM_011511687.1:c.1413+81_1413+85dup XP_011509989.1:n.1413+81_1413+85dup
XM_011511688.1:c.1413+81_1413+85dup XP_011509990.1:n.1413+81_1413+85dup
NM_001204.7:c.1413+81_1413+85dup MANE Select NP_001195.2:n.1413+81_1413+85dup