Canonical Allele Identifier: CA2036266983

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913177G= , CM000674.2:g.51913177G=	GRCh38
NC_000012.11:g.52306961G= , CM000674.1:g.52306961G=	GRCh37
NC_000012.10:g.50593228G=	NCBI36
NG_009549.1:g.10760G= , LRG_543:g.10760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.182G=	ENSP00000446724.2:p.Arg61=
ENST00000551576.6:c.140G=	ENSP00000455848.2:p.Arg47=
ENST00000552678.2:c.140G=	ENSP00000457394.2:p.Arg47=
ENST00000388922.9:c.140G= MANE Select	ENSP00000373574.4:p.Arg47=
ENST00000388922.8:c.140G=	ENSP00000373574.4:p.Arg47=
ENST00000419526.6:c.103+642G=	ENSP00000392492.2:n.103+642G=
ENST00000547400.5:c.182G=	ENSP00000446724.1:p.Arg61=
ENST00000550683.5:c.182G=	ENSP00000447884.1:p.Arg61=
ENST00000551576.5:c.140G=	ENSP00000455848.1:p.Arg47=
NM_000020.2:c.140G= , LRG_543t1:c.140G=	NP_000011.2:p.Arg47=
NM_001077401.1:c.140G=	NP_001070869.1:p.Arg47=
XM_005269235.2:c.140G=	XP_005269292.1:p.Arg47=
XM_011539008.1:c.182G=	XP_011537310.1:p.Arg61=
NM_000020.3:c.140G= MANE Select	NP_000011.2:p.Arg47=
NM_001077401.2:c.140G=	NP_001070869.1:p.Arg47=