Canonical Allele Identifier: CA1321544847

Gene: BMPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202530688_202530692delinsAAATT , CM000664.2:g.202530688_202530692delinsAAATT	GRCh38
NC_000002.11:g.203395411_203395415delinsAAATT , CM000664.1:g.203395411_203395415delinsAAATT	GRCh37
NC_000002.10:g.203103656_203103660delinsAAATT	NCBI36
NG_009363.1:g.159362_159366delinsAAATT , LRG_712:g.159362_159366delinsAAATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000374580.10:c.968-106_968-102delinsAAATT MANE Select	ENSP00000363708.4:n.968-106_968-102delins...
ENST00000638587.1:c.899-106_899-102delinsAAATT	ENSP00000491062.1:n.899-106_899-102delins...
ENST00000374574.2:c.968-106_968-102delinsAAATT	ENSP00000363702.2:n.968-106_968-102delins...
ENST00000374580.8:c.968-106_968-102delinsAAATT	ENSP00000363708.4:n.968-106_968-102delins...
NM_001204.6:c.968-106_968-102delinsAAATT , LRG_712t1:c.968-106_968-102delinsAAATT	NP_001195.2:n.968-106_968-102delinsAAATT
XM_011511687.1:c.968-106_968-102delinsAAATT	XP_011509989.1:n.968-106_968-102delinsAAA...
XM_011511688.1:c.968-106_968-102delinsAAATT	XP_011509990.1:n.968-106_968-102delinsAAA...
NM_001204.7:c.968-106_968-102delinsAAATT MANE Select	NP_001195.2:n.968-106_968-102delinsAAATT