Canonical Allele Identifier: CA1321544858
Gene: BMPR2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530714_202530717delinsACTT , CM000664.2:g.202530714_202530717delinsACTT GRCh38
NC_000002.11:g.203395437_203395440delinsACTT , CM000664.1:g.203395437_203395440delinsACTT GRCh37
NC_000002.10:g.203103682_203103685delinsACTT NCBI36
NG_009363.1:g.159388_159391delinsACTT , LRG_712:g.159388_159391delinsACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-80_968-77delinsACTT MANE Select ENSP00000363708.4:n.968-80_968-77delinsACTT
ENST00000638587.1:c.899-80_899-77delinsACTT ENSP00000491062.1:n.899-80_899-77delinsACTT
ENST00000374574.2:c.968-80_968-77delinsACTT ENSP00000363702.2:n.968-80_968-77delinsACTT
ENST00000374580.8:c.968-80_968-77delinsACTT ENSP00000363708.4:n.968-80_968-77delinsACTT
NM_001204.6:c.968-80_968-77delinsACTT , LRG_712t1:c.968-80_968-77delinsACTT NP_001195.2:n.968-80_968-77delinsACTT
XM_011511687.1:c.968-80_968-77delinsACTT XP_011509989.1:n.968-80_968-77delinsACTT
XM_011511688.1:c.968-80_968-77delinsACTT XP_011509990.1:n.968-80_968-77delinsACTT
NM_001204.7:c.968-80_968-77delinsACTT MANE Select NP_001195.2:n.968-80_968-77delinsACTT
Search 100 bp 5'
Search 100 bp 3'