Canonical Allele Identifier: CA1925653009
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86756817_86756850delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT , CM000672.2:g.86756817_86756850delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT GRCh38
NC_000010.10:g.88516574_88516607delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT , CM000672.1:g.88516574_88516607delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT GRCh37
NC_000010.9:g.88506554_88506587delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT NCBI36
NG_009362.1:g.5179_5212delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT , LRG_298:g.5179_5212delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT ENSP00000483569.2:n.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGG...
ENST00000635816.2:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT ENSP00000489707.1:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGG...
ENST00000636056.2:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT ENSP00000490273.1:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGG...
ENST00000372037.8:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT MANE Select ENSP00000361107.2:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGG...
ENST00000638429.1:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT ENSP00000492290.1:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGG...
ENST00000372037.7:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT ENSP00000361107.1:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGG...
NM_004329.2:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT , LRG_298t1:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT NP_004320.2:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCAC...
XM_011540103.1:c.-268+854_-268+887delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT XP_011538405.1:n.-268+854_-268+887delinsACGCCAAGGGCGAAGGCCGAT...
XM_011540104.1:c.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT XP_011538406.1:n.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGGCCC...
XM_011540103.2:c.-268+854_-268+887delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT XP_011538405.1:n.-268+854_-268+887delinsACGCCAAGGGCGAAGGCCGAT...
XM_011540104.2:c.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT XP_011538406.1:n.-475_-442delinsACGCCAAGGGCGAAGGCCGATTCGGGCCC...
NM_004329.3:c.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTT MANE Select NP_004320.2:n.-370_-337delinsACGCCAAGGGCGAAGGCCGATTCGGGCCCCAC...