Canonical Allele Identifier: CA1321540051

Gene: BMPR2

Linked Data

• dbSNP Id: rs1687786903

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202519751_202519752insGTTGC , CM000664.2:g.202519751_202519752insGTTGC	GRCh38
NC_000002.11:g.203384474_203384475insGTTGC , CM000664.1:g.203384474_203384475insGTTGC	GRCh37
NC_000002.10:g.203092719_203092720insGTTGC	NCBI36
NG_009363.1:g.148425_148426insGTTGC , LRG_712:g.148425_148426insGTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.853-336_853-335insGTTGC MANE Select	ENSP00000363708.4:n.853-336_853-335insGTTGC
ENST00000638587.1:c.784-336_784-335insGTTGC	ENSP00000491062.1:n.784-336_784-335insGTTGC
ENST00000374574.2:c.853-336_853-335insGTTGC	ENSP00000363702.2:n.853-336_853-335insGTTGC
ENST00000374580.8:c.853-336_853-335insGTTGC	ENSP00000363708.4:n.853-336_853-335insGTTGC
NM_001204.6:c.853-336_853-335insGTTGC , LRG_712t1:c.853-336_853-335insGTTGC	NP_001195.2:n.853-336_853-335insGTTGC
XM_011511687.1:c.853-336_853-335insGTTGC	XP_011509989.1:n.853-336_853-335insGTTGC
XM_011511688.1:c.853-336_853-335insGTTGC	XP_011509990.1:n.853-336_853-335insGTTGC
NM_001204.7:c.853-336_853-335insGTTGC MANE Select	NP_001195.2:n.853-336_853-335insGTTGC