Canonical Allele Identifier: CA2506561814
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86842606G>T , CM000672.2:g.86842606G>T GRCh38
NC_000010.10:g.88602363G>T , CM000672.1:g.88602363G>T GRCh37
NC_000010.9:g.88592343G>T NCBI36
NG_009362.1:g.90968G>T , LRG_298:g.90968G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000480152.3:c.-257-800G>T ENSP00000483569.2:n.-257-800G>T
ENST00000635816.2:c.-153+3627G>T ENSP00000489707.1:n.-153+3627G>T
ENST00000636056.2:c.-153+3627G>T ENSP00000490273.1:n.-153+3627G>T
ENST00000372037.8:c.-153+3627G>T MANE Select ENSP00000361107.2:n.-153+3627G>T
ENST00000635816.1:c.-153+3627G>T ENSP00000489707.1:n.-153+3627G>T
ENST00000636056.1:c.-153+3627G>T ENSP00000490273.1:n.-153+3627G>T
ENST00000638429.1:c.-153+3627G>T ENSP00000492290.1:n.-153+3627G>T
ENST00000372037.7:c.-153+3627G>T ENSP00000361107.1:n.-153+3627G>T
ENST00000480152.2:c.-257-800G>T ENSP00000483569.1:n.-257-800G>T
NM_004329.2:c.-153+3627G>T , LRG_298t1:c.-153+3627G>T NP_004320.2:n.-153+3627G>T
XM_011540103.1:c.-153+3627G>T XP_011538405.1:n.-153+3627G>T
XM_011540104.1:c.-257-800G>T XP_011538406.1:n.-257-800G>T
XM_011540103.2:c.-153+3627G>T XP_011538405.1:n.-153+3627G>T
XM_011540104.2:c.-257-800G>T XP_011538406.1:n.-257-800G>T
NM_004329.3:c.-153+3627G>T MANE Select NP_004320.2:n.-153+3627G>T