Canonical Allele Identifier: CA2662706009

Gene: BMPR2

Linked Data

• gnomAD v4: 2-202520215-T-TTTCATCTATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202520215_202520216insTTCATCTATTG , CM000664.2:g.202520215_202520216insTTCATCTATTG	GRCh38
NC_000002.11:g.203384938_203384939insTTCATCTATTG , CM000664.1:g.203384938_203384939insTTCATCTATTG	GRCh37
NC_000002.10:g.203093183_203093184insTTCATCTATTG	NCBI36
NG_009363.1:g.148889_148890insTTCATCTATTG , LRG_712:g.148889_148890insTTCATCTATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.967+14_967+15insTTCATCTATTG MANE Select	ENSP00000363708.4:n.967+14_967+15insTTCATCTATTG
ENST00000638587.1:c.898+14_898+15insTTCATCTATTG	ENSP00000491062.1:n.898+14_898+15insTTCATCTATTG
ENST00000374574.2:c.967+14_967+15insTTCATCTATTG	ENSP00000363702.2:n.967+14_967+15insTTCATCTATTG
ENST00000374580.8:c.967+14_967+15insTTCATCTATTG	ENSP00000363708.4:n.967+14_967+15insTTCATCTATTG
NM_001204.6:c.967+14_967+15insTTCATCTATTG , LRG_712t1:c.967+14_967+15insTTCATCTATTG	NP_001195.2:n.967+14_967+15insTTCATCTATTG
XM_011511687.1:c.967+14_967+15insTTCATCTATTG	XP_011509989.1:n.967+14_967+15insTTCATCTATTG
XM_011511688.1:c.967+14_967+15insTTCATCTATTG	XP_011509990.1:n.967+14_967+15insTTCATCTATTG
NM_001204.7:c.967+14_967+15insTTCATCTATTG MANE Select	NP_001195.2:n.967+14_967+15insTTCATCTATTG