Canonical Allele Identifier: CA1925714497
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86899782_86899785delinsCTCT , CM000672.2:g.86899782_86899785delinsCTCT GRCh38
NC_000010.10:g.88659539_88659542delinsCTCT , CM000672.1:g.88659539_88659542delinsCTCT GRCh37
NC_000010.9:g.88649519_88649522delinsCTCT NCBI36
NG_009362.1:g.148144_148147delinsCTCT , LRG_298:g.148144_148147delinsCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.334-12_334-9delinsCTCT ENSP00000483569.2:n.334-12_334-9delinsCTCT
ENST00000635816.2:c.334-12_334-9delinsCTCT ENSP00000489707.1:n.334-12_334-9delinsCTCT
ENST00000636056.2:c.334-12_334-9delinsCTCT ENSP00000490273.1:n.334-12_334-9delinsCTCT
ENST00000372037.8:c.334-12_334-9delinsCTCT MANE Select ENSP00000361107.2:n.334-12_334-9delinsCTCT
ENST00000635816.1:c.334-12_334-9delinsCTCT ENSP00000489707.1:n.334-12_334-9delinsCTCT
ENST00000636056.1:c.334-12_334-9delinsCTCT ENSP00000490273.1:n.334-12_334-9delinsCTCT
ENST00000638429.1:c.334-12_334-9delinsCTCT ENSP00000492290.1:n.334-12_334-9delinsCTCT
ENST00000372037.7:c.334-12_334-9delinsCTCT ENSP00000361107.1:n.334-12_334-9delinsCTCT
NM_004329.2:c.334-12_334-9delinsCTCT , LRG_298t1:c.334-12_334-9delinsCTCT NP_004320.2:n.334-12_334-9delinsCTCT
XM_011540103.1:c.334-12_334-9delinsCTCT XP_011538405.1:n.334-12_334-9delinsCTCT
XM_011540104.1:c.334-12_334-9delinsCTCT XP_011538406.1:n.334-12_334-9delinsCTCT
XM_011540103.2:c.334-12_334-9delinsCTCT XP_011538405.1:n.334-12_334-9delinsCTCT
XM_011540104.2:c.334-12_334-9delinsCTCT XP_011538406.1:n.334-12_334-9delinsCTCT
NM_004329.3:c.334-12_334-9delinsCTCT MANE Select NP_004320.2:n.334-12_334-9delinsCTCT