Canonical Allele Identifier: CA1925692717
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86842487T= , CM000672.2:g.86842487T= GRCh38
NC_000010.10:g.88602244T= , CM000672.1:g.88602244T= GRCh37
NC_000010.9:g.88592224T= NCBI36
NG_009362.1:g.90849T= , LRG_298:g.90849T=

Transcript Alleles

HGVS Amino-acid change
ENST00000480152.3:c.-257-919T= ENSP00000483569.2:n.-257-919T=
ENST00000635816.2:c.-153+3508T= ENSP00000489707.1:n.-153+3508T=
ENST00000636056.2:c.-153+3508T= ENSP00000490273.1:n.-153+3508T=
ENST00000372037.8:c.-153+3508T= MANE Select ENSP00000361107.2:n.-153+3508T=
ENST00000635816.1:c.-153+3508T= ENSP00000489707.1:n.-153+3508T=
ENST00000636056.1:c.-153+3508T= ENSP00000490273.1:n.-153+3508T=
ENST00000638429.1:c.-153+3508T= ENSP00000492290.1:n.-153+3508T=
ENST00000372037.7:c.-153+3508T= ENSP00000361107.1:n.-153+3508T=
ENST00000480152.2:c.-257-919T= ENSP00000483569.1:n.-257-919T=
NM_004329.2:c.-153+3508T= , LRG_298t1:c.-153+3508T= NP_004320.2:n.-153+3508T=
XM_011540103.1:c.-153+3508T= XP_011538405.1:n.-153+3508T=
XM_011540104.1:c.-257-919T= XP_011538406.1:n.-257-919T=
XM_011540103.2:c.-153+3508T= XP_011538405.1:n.-153+3508T=
XM_011540104.2:c.-257-919T= XP_011538406.1:n.-257-919T=
NM_004329.3:c.-153+3508T= MANE Select NP_004320.2:n.-153+3508T=