Canonical Allele Identifier: CA1925715300

Gene: BMPR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86900098_86900104delinsATCATCT , CM000672.2:g.86900098_86900104delinsATCATCT	GRCh38
NC_000010.10:g.88659855_88659861delinsATCATCT , CM000672.1:g.88659855_88659861delinsATCATCT	GRCh37
NC_000010.9:g.88649835_88649841delinsATCATCT	NCBI36
NG_009362.1:g.148460_148466delinsATCATCT , LRG_298:g.148460_148466delinsATCATCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000480152.3:c.502_508delinsATCATCT	ENSP00000483569.2:p.Ile168=
ENST00000635816.2:c.502_508delinsATCATCT	ENSP00000489707.1:p.Ile168=
ENST00000636056.2:c.502_508delinsATCATCT	ENSP00000490273.1:p.Ile168=
ENST00000372037.8:c.502_508delinsATCATCT MANE Select	ENSP00000361107.2:p.Ile168=
ENST00000635816.1:c.502_508delinsATCATCT	ENSP00000489707.1:p.Ile168=
ENST00000636056.1:c.502_508delinsATCATCT	ENSP00000490273.1:p.Ile168=
ENST00000638429.1:c.502_508delinsATCATCT	ENSP00000492290.1:p.Ile168=
ENST00000372037.7:c.502_508delinsATCATCT	ENSP00000361107.1:p.Ile168=
NM_004329.2:c.502_508delinsATCATCT , LRG_298t1:c.502_508delinsATCATCT	NP_004320.2:p.Ile168=
XM_011540103.1:c.502_508delinsATCATCT	XP_011538405.1:p.Ile168=
XM_011540104.1:c.502_508delinsATCATCT	XP_011538406.1:p.Ile168=
XM_011540103.2:c.502_508delinsATCATCT	XP_011538405.1:p.Ile168=
XM_011540104.2:c.502_508delinsATCATCT	XP_011538406.1:p.Ile168=
NM_004329.3:c.502_508delinsATCATCT MANE Select	NP_004320.2:p.Ile168=