Canonical Allele Identifier: CA2662706532

Gene: BMPR2

Linked Data

• gnomAD v4: 2-202552579-C-CTATG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202552581_202552582insTGTA , CM000664.2:g.202552581_202552582insTGTA	GRCh38
NC_000002.11:g.203417304_203417305insTGTA , CM000664.1:g.203417304_203417305insTGTA	GRCh37
NC_000002.10:g.203125549_203125550insTGTA	NCBI36
NG_009363.1:g.181255_181256insTGTA , LRG_712:g.181255_181256insTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.1414-135_1414-134insTGTA MANE Select	ENSP00000363708.4:n.1414-135_1414-134insTGTA
ENST00000638587.1:c.1345-135_1345-134insTGTA	ENSP00000491062.1:n.1345-135_1345-134insTGTA
ENST00000374574.2:c.1414-135_1414-134insTGTA	ENSP00000363702.2:n.1414-135_1414-134insTGTA
ENST00000374580.8:c.1414-135_1414-134insTGTA	ENSP00000363708.4:n.1414-135_1414-134insTGTA
NM_001204.6:c.1414-135_1414-134insTGTA , LRG_712t1:c.1414-135_1414-134insTGTA	NP_001195.2:n.1414-135_1414-134insTGTA
XM_011511687.1:c.1414-135_1414-134insTGTA	XP_011509989.1:n.1414-135_1414-134insTGTA
XM_011511688.1:c.1414-135_1414-134insTGTA	XP_011509990.1:n.1414-135_1414-134insTGTA
NM_001204.7:c.1414-135_1414-134insTGTA MANE Select	NP_001195.2:n.1414-135_1414-134insTGTA