Canonical Allele Identifier: CA1925652856

Gene: BMPR1A

Linked Data

• dbSNP Id: rs1847873567

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86756743_86756744insC , CM000672.2:g.86756743_86756744insC	GRCh38
NC_000010.10:g.88516500_88516501insC , CM000672.1:g.88516500_88516501insC	GRCh37
NC_000010.9:g.88506480_88506481insC	NCBI36
NG_009362.1:g.5105_5106insC , LRG_298:g.5105_5106insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-549_-548insC	ENSP00000483569.2:n.-549_-548insC
ENST00000635816.2:c.-444_-443insC	ENSP00000489707.1:n.-444_-443insC
ENST00000636056.2:c.-444_-443insC	ENSP00000490273.1:n.-444_-443insC
ENST00000372037.8:c.-444_-443insC MANE Select	ENSP00000361107.2:n.-444_-443insC
ENST00000638429.1:c.-444_-443insC	ENSP00000492290.1:n.-444_-443insC
ENST00000372037.7:c.-444_-443insC	ENSP00000361107.1:n.-444_-443insC
NM_004329.2:c.-444_-443insC , LRG_298t1:c.-444_-443insC	NP_004320.2:n.-444_-443insC
XM_011540103.1:c.-268+780_-268+781insC	XP_011538405.1:n.-268+780_-268+781insC
XM_011540104.1:c.-549_-548insC	XP_011538406.1:n.-549_-548insC
XM_011540103.2:c.-268+780_-268+781insC	XP_011538405.1:n.-268+780_-268+781insC
XM_011540104.2:c.-549_-548insC	XP_011538406.1:n.-549_-548insC
NM_004329.3:c.-444_-443insC MANE Select	NP_004320.2:n.-444_-443insC