Canonical Allele Identifier: CA5585533
Gene: BMPR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 665773
dbSNP Id: rs763934014

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86900091T>G , CM000672.2:g.86900091T>G GRCh38
NC_000010.10:g.88659848T>G , CM000672.1:g.88659848T>G GRCh37
NC_000010.9:g.88649828T>G NCBI36
NG_009362.1:g.148453T>G , LRG_298:g.148453T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.495T>G ENSP00000483569.2:p.Ile165Met
ENST00000635816.2:c.495T>G ENSP00000489707.1:p.Ile165Met
ENST00000636056.2:c.495T>G ENSP00000490273.1:p.Ile165Met
ENST00000372037.8:c.495T>G MANE Select ENSP00000361107.2:p.Ile165Met
ENST00000635816.1:c.495T>G ENSP00000489707.1:p.Ile165Met
ENST00000636056.1:c.495T>G ENSP00000490273.1:p.Ile165Met
ENST00000638429.1:c.495T>G ENSP00000492290.1:p.Ile165Met
ENST00000372037.7:c.495T>G ENSP00000361107.1:p.Ile165Met
NM_004329.2:c.495T>G , LRG_298t1:c.495T>G NP_004320.2:p.Ile165Met
XM_011540103.1:c.495T>G XP_011538405.1:p.Ile165Met
XM_011540104.1:c.495T>G XP_011538406.1:p.Ile165Met
XM_011540103.2:c.495T>G XP_011538405.1:p.Ile165Met
XM_011540104.2:c.495T>G XP_011538406.1:p.Ile165Met
NM_004329.3:c.495T>G MANE Select NP_004320.2:p.Ile165Met