Canonical Allele Identifier: CA1925652843

Gene: BMPR1A

Linked Data

• dbSNP Id: rs1847873337

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86756740_86756741insCGTC , CM000672.2:g.86756740_86756741insCGTC	GRCh38
NC_000010.10:g.88516497_88516498insCGTC , CM000672.1:g.88516497_88516498insCGTC	GRCh37
NC_000010.9:g.88506477_88506478insCGTC	NCBI36
NG_009362.1:g.5102_5103insCGTC , LRG_298:g.5102_5103insCGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000480152.3:c.-552_-551insCGTC	ENSP00000483569.2:n.-552_-551insCGTC
ENST00000635816.2:c.-447_-446insCGTC	ENSP00000489707.1:n.-447_-446insCGTC
ENST00000636056.2:c.-447_-446insCGTC	ENSP00000490273.1:n.-447_-446insCGTC
ENST00000372037.8:c.-447_-446insCGTC MANE Select	ENSP00000361107.2:n.-447_-446insCGTC
ENST00000638429.1:c.-447_-446insCGTC	ENSP00000492290.1:n.-447_-446insCGTC
ENST00000372037.7:c.-447_-446insCGTC	ENSP00000361107.1:n.-447_-446insCGTC
NM_004329.2:c.-447_-446insCGTC , LRG_298t1:c.-447_-446insCGTC	NP_004320.2:n.-447_-446insCGTC
XM_011540103.1:c.-268+777_-268+778insCGTC	XP_011538405.1:n.-268+777_-268+778insCGTC
XM_011540104.1:c.-552_-551insCGTC	XP_011538406.1:n.-552_-551insCGTC
XM_011540103.2:c.-268+777_-268+778insCGTC	XP_011538405.1:n.-268+777_-268+778insCGTC
XM_011540104.2:c.-552_-551insCGTC	XP_011538406.1:n.-552_-551insCGTC
NM_004329.3:c.-447_-446insCGTC MANE Select	NP_004320.2:n.-447_-446insCGTC