Canonical Allele Identifier: CA1925653375
Gene: BMPR1A HGNC NCBI

Linked Data

dbSNP Id: rs1847882080

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86757026_86757047dup , CM000672.2:g.86757026_86757047dup GRCh38
NC_000010.10:g.88516783_88516804dup , CM000672.1:g.88516783_88516804dup GRCh37
NC_000010.9:g.88506763_88506784dup NCBI36
NG_009362.1:g.5388_5409dup , LRG_298:g.5388_5409dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.-373+107_-373+128dup ENSP00000483569.2:n.-373+107_-373+128dup
ENST00000635816.2:c.-268+107_-268+128dup ENSP00000489707.1:n.-268+107_-268+128dup
ENST00000636056.2:c.-268+107_-268+128dup ENSP00000490273.1:n.-268+107_-268+128dup
ENST00000372037.8:c.-268+107_-268+128dup MANE Select ENSP00000361107.2:n.-268+107_-268+128dup
ENST00000638429.1:c.-268+107_-268+128dup ENSP00000492290.1:n.-268+107_-268+128dup
ENST00000372037.7:c.-268+107_-268+128dup ENSP00000361107.1:n.-268+107_-268+128dup
NM_004329.2:c.-268+107_-268+128dup , LRG_298t1:c.-268+107_-268+128dup NP_004320.2:n.-268+107_-268+128dup
XM_011540103.1:c.-268+1063_-268+1084dup XP_011538405.1:n.-268+1063_-268+1084dup
XM_011540104.1:c.-373+107_-373+128dup XP_011538406.1:n.-373+107_-373+128dup
XM_011540103.2:c.-268+1063_-268+1084dup XP_011538405.1:n.-268+1063_-268+1084dup
XM_011540104.2:c.-373+107_-373+128dup XP_011538406.1:n.-373+107_-373+128dup
NM_004329.3:c.-268+107_-268+128dup MANE Select NP_004320.2:n.-268+107_-268+128dup