Canonical Allele Identifier: CA1321556962

Gene: BMPR2

Linked Data

• dbSNP Id: rs1688511347

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202553153_202553154insT , CM000664.2:g.202553153_202553154insT	GRCh38
NC_000002.11:g.203417876_203417877insT , CM000664.1:g.203417876_203417877insT	GRCh37
NC_000002.10:g.203126121_203126122insT	NCBI36
NG_009363.1:g.181827_181828insT , LRG_712:g.181827_181828insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.1586+265_1586+266insT MANE Select	ENSP00000363708.4:n.1586+265_1586+266insT
ENST00000638587.1:c.1517+265_1517+266insT	ENSP00000491062.1:n.1517+265_1517+266insT
ENST00000374574.2:c.1586+265_1586+266insT	ENSP00000363702.2:n.1586+265_1586+266insT
ENST00000374580.8:c.1586+265_1586+266insT	ENSP00000363708.4:n.1586+265_1586+266insT
NM_001204.6:c.1586+265_1586+266insT , LRG_712t1:c.1586+265_1586+266insT	NP_001195.2:n.1586+265_1586+266insT
XM_011511687.1:c.1586+265_1586+266insT	XP_011509989.1:n.1586+265_1586+266insT
XM_011511688.1:c.1586+265_1586+266insT	XP_011509990.1:n.1586+265_1586+266insT
NM_001204.7:c.1586+265_1586+266insT MANE Select	NP_001195.2:n.1586+265_1586+266insT