Canonical Allele Identifier: CA1629822331

Gene: BMP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55844943C= , CM000668.2:g.55844943C=	GRCh38
NC_000006.11:g.55709741C= , CM000668.1:g.55709741C=	GRCh37
NC_000006.10:g.55817700C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021073.4:c.491-25096G= MANE Select	NP_066551.1:n.491-25096G=
ENST00000370830.4:c.491-25096G= MANE Select	ENSP00000359866.3:n.491-25096G=
NM_001329754.1:c.491-25096G=	NP_001316683.1:n.491-25096G=
NM_001329754.2:c.491-25096G=	NP_001316683.1:n.491-25096G=
NM_001329756.1:c.491-25096G=	NP_001316685.1:n.491-25096G=
NM_001329756.2:c.491-25096G=	NP_001316685.1:n.491-25096G=
NM_021073.2:c.491-25096G=	NP_066551.1:n.491-25096G=
NM_021073.3:c.491-25096G=	NP_066551.1:n.491-25096G=
ENST00000370830.3:c.491-25096G=	ENSP00000359866.3:n.491-25096G=
XM_005249304.2:c.491-25096G=	XP_005249361.1:n.491-25096G=
XM_011514816.1:c.491-25096G=	XP_011513118.1:n.491-25096G=
XM_011514817.1:c.491-25096G=	XP_011513119.1:n.491-25096G=
XM_011514817.3:c.491-25096G=	XP_011513119.1:n.491-25096G=
XM_024446524.1:c.491-25096G=	XP_024302292.1:n.491-25096G=