Canonical Allele Identifier: CA2036267041

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913213A= , CM000674.2:g.51913213A=	GRCh38
NC_000012.11:g.52306997A= , CM000674.1:g.52306997A=	GRCh37
NC_000012.10:g.50593264A=	NCBI36
NG_009549.1:g.10796A= , LRG_543:g.10796A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.218A=	ENSP00000446724.2:p.Glu73=
ENST00000551576.6:c.176A=	ENSP00000455848.2:p.Glu59=
ENST00000552678.2:c.176A=	ENSP00000457394.2:p.Glu59=
ENST00000388922.9:c.176A= MANE Select	ENSP00000373574.4:p.Glu59=
ENST00000388922.8:c.176A=	ENSP00000373574.4:p.Glu59=
ENST00000419526.6:c.103+678A=	ENSP00000392492.2:n.103+678A=
ENST00000547400.5:c.218A=	ENSP00000446724.1:p.Glu73=
ENST00000550683.5:c.218A=	ENSP00000447884.1:p.Glu73=
ENST00000551576.5:c.176A=	ENSP00000455848.1:p.Glu59=
NM_000020.2:c.176A= , LRG_543t1:c.176A=	NP_000011.2:p.Glu59=
NM_001077401.1:c.176A=	NP_001070869.1:p.Glu59=
XM_005269235.2:c.176A=	XP_005269292.1:p.Glu59=
XM_011539008.1:c.218A=	XP_011537310.1:p.Glu73=
NM_000020.3:c.176A= MANE Select	NP_000011.2:p.Glu59=
NM_001077401.2:c.176A=	NP_001070869.1:p.Glu59=