Canonical Allele Identifier: CA2036266238

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51912479C= , CM000674.2:g.51912479C=	GRCh38
NC_000012.11:g.52306263C= , CM000674.1:g.52306263C=	GRCh37
NC_000012.10:g.50592530C=	NCBI36
NG_009549.1:g.10062C= , LRG_543:g.10062C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.47C=	ENSP00000446724.2:p.Thr16=
ENST00000551576.6:c.5C=	ENSP00000455848.2:p.Thr2=
ENST00000552678.2:c.5C=	ENSP00000457394.2:p.Thr2=
ENST00000388922.9:c.5C= MANE Select	ENSP00000373574.4:p.Thr2=
ENST00000388922.8:c.5C=	ENSP00000373574.4:p.Thr2=
ENST00000419526.6:c.47C=	ENSP00000392492.2:p.Thr16=
ENST00000547400.5:c.47C=	ENSP00000446724.1:p.Thr16=
ENST00000550683.5:c.47C=	ENSP00000447884.1:p.Thr16=
ENST00000551576.5:c.5C=	ENSP00000455848.1:p.Thr2=
NM_000020.2:c.5C= , LRG_543t1:c.5C=	NP_000011.2:p.Thr2=
NM_001077401.1:c.5C=	NP_001070869.1:p.Thr2=
XM_005269235.2:c.5C=	XP_005269292.1:p.Thr2=
XM_011539008.1:c.47C=	XP_011537310.1:p.Thr16=
NM_000020.3:c.5C= MANE Select	NP_000011.2:p.Thr2=
NM_001077401.2:c.5C=	NP_001070869.1:p.Thr2=