Canonical Allele Identifier: CA1321540171

Gene: BMPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202520024_202520027delinsCTCT , CM000664.2:g.202520024_202520027delinsCTCT	GRCh38
NC_000002.11:g.203384747_203384750delinsCTCT , CM000664.1:g.203384747_203384750delinsCTCT	GRCh37
NC_000002.10:g.203092992_203092995delinsCTCT	NCBI36
NG_009363.1:g.148698_148701delinsCTCT , LRG_712:g.148698_148701delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.853-63_853-60delinsCTCT MANE Select	ENSP00000363708.4:n.853-63_853-60delinsCTCT
ENST00000638587.1:c.784-63_784-60delinsCTCT	ENSP00000491062.1:n.784-63_784-60delinsCTCT
ENST00000374574.2:c.853-63_853-60delinsCTCT	ENSP00000363702.2:n.853-63_853-60delinsCTCT
ENST00000374580.8:c.853-63_853-60delinsCTCT	ENSP00000363708.4:n.853-63_853-60delinsCTCT
NM_001204.6:c.853-63_853-60delinsCTCT , LRG_712t1:c.853-63_853-60delinsCTCT	NP_001195.2:n.853-63_853-60delinsCTCT
XM_011511687.1:c.853-63_853-60delinsCTCT	XP_011509989.1:n.853-63_853-60delinsCTCT
XM_011511688.1:c.853-63_853-60delinsCTCT	XP_011509990.1:n.853-63_853-60delinsCTCT
NM_001204.7:c.853-63_853-60delinsCTCT MANE Select	NP_001195.2:n.853-63_853-60delinsCTCT