Canonical Allele Identifier: CA1925653628
Gene: BMPR1A HGNC NCBI

Linked Data

dbSNP Id: rs1847887502
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86757198dup , CM000672.2:g.86757198dup GRCh38
NC_000010.10:g.88516955dup , CM000672.1:g.88516955dup GRCh37
NC_000010.9:g.88506935dup NCBI36
NG_009362.1:g.5560dup , LRG_298:g.5560dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.-373+279dup ENSP00000483569.2:n.-373+279dup
ENST00000635816.2:c.-268+279dup ENSP00000489707.1:n.-268+279dup
ENST00000636056.2:c.-268+279dup ENSP00000490273.1:n.-268+279dup
ENST00000372037.8:c.-268+279dup MANE Select ENSP00000361107.2:n.-268+279dup
ENST00000638429.1:c.-268+279dup ENSP00000492290.1:n.-268+279dup
ENST00000372037.7:c.-268+279dup ENSP00000361107.1:n.-268+279dup
NM_004329.2:c.-268+279dup , LRG_298t1:c.-268+279dup NP_004320.2:n.-268+279dup
XM_011540103.1:c.-268+1235dup XP_011538405.1:n.-268+1235dup
XM_011540104.1:c.-373+279dup XP_011538406.1:n.-373+279dup
XM_011540103.2:c.-268+1235dup XP_011538405.1:n.-268+1235dup
XM_011540104.2:c.-373+279dup XP_011538406.1:n.-373+279dup
NM_004329.3:c.-268+279dup MANE Select NP_004320.2:n.-268+279dup
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