Canonical Allele Identifier: CA1925692808
Gene: BMPR1A HGNC NCBI

Linked Data

dbSNP Id: rs11202222

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86842729C>A , CM000672.2:g.86842729C>A GRCh38
NC_000010.10:g.88602486C>A , CM000672.1:g.88602486C>A GRCh37
NC_000010.9:g.88592466C>A NCBI36
NG_009362.1:g.91091C>A , LRG_298:g.91091C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000480152.3:c.-257-677C>A ENSP00000483569.2:n.-257-677C>A
ENST00000635816.2:c.-153+3750C>A ENSP00000489707.1:n.-153+3750C>A
ENST00000636056.2:c.-153+3750C>A ENSP00000490273.1:n.-153+3750C>A
ENST00000372037.8:c.-153+3750C>A MANE Select ENSP00000361107.2:n.-153+3750C>A
ENST00000635816.1:c.-153+3750C>A ENSP00000489707.1:n.-153+3750C>A
ENST00000636056.1:c.-153+3750C>A ENSP00000490273.1:n.-153+3750C>A
ENST00000638429.1:c.-153+3750C>A ENSP00000492290.1:n.-153+3750C>A
ENST00000372037.7:c.-153+3750C>A ENSP00000361107.1:n.-153+3750C>A
ENST00000480152.2:c.-257-677C>A ENSP00000483569.1:n.-257-677C>A
NM_004329.2:c.-153+3750C>A , LRG_298t1:c.-153+3750C>A NP_004320.2:n.-153+3750C>A
XM_011540103.1:c.-153+3750C>A XP_011538405.1:n.-153+3750C>A
XM_011540104.1:c.-257-677C>A XP_011538406.1:n.-257-677C>A
XM_011540103.2:c.-153+3750C>A XP_011538405.1:n.-153+3750C>A
XM_011540104.2:c.-257-677C>A XP_011538406.1:n.-257-677C>A
NM_004329.3:c.-153+3750C>A MANE Select NP_004320.2:n.-153+3750C>A