Canonical Allele Identifier: CA1321540202

Gene: BMPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202520075_202520077delinsTCC , CM000664.2:g.202520075_202520077delinsTCC	GRCh38
NC_000002.11:g.203384798_203384800delinsTCC , CM000664.1:g.203384798_203384800delinsTCC	GRCh37
NC_000002.10:g.203093043_203093045delinsTCC	NCBI36
NG_009363.1:g.148749_148751delinsTCC , LRG_712:g.148749_148751delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.853-12_853-10delinsTCC MANE Select	ENSP00000363708.4:n.853-12_853-10delinsTCC
ENST00000638587.1:c.784-12_784-10delinsTCC	ENSP00000491062.1:n.784-12_784-10delinsTCC
ENST00000374574.2:c.853-12_853-10delinsTCC	ENSP00000363702.2:n.853-12_853-10delinsTCC
ENST00000374580.8:c.853-12_853-10delinsTCC	ENSP00000363708.4:n.853-12_853-10delinsTCC
NM_001204.6:c.853-12_853-10delinsTCC , LRG_712t1:c.853-12_853-10delinsTCC	NP_001195.2:n.853-12_853-10delinsTCC
XM_011511687.1:c.853-12_853-10delinsTCC	XP_011509989.1:n.853-12_853-10delinsTCC
XM_011511688.1:c.853-12_853-10delinsTCC	XP_011509990.1:n.853-12_853-10delinsTCC
NM_001204.7:c.853-12_853-10delinsTCC MANE Select	NP_001195.2:n.853-12_853-10delinsTCC