Canonical Allele Identifier: CA2036267003

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913183C= , CM000674.2:g.51913183C=	GRCh38
NC_000012.11:g.52306967C= , CM000674.1:g.52306967C=	GRCh37
NC_000012.10:g.50593234C=	NCBI36
NG_009549.1:g.10766C= , LRG_543:g.10766C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.188C=	ENSP00000446724.2:p.Ala63=
ENST00000551576.6:c.146C=	ENSP00000455848.2:p.Ala49=
ENST00000552678.2:c.146C=	ENSP00000457394.2:p.Ala49=
ENST00000388922.9:c.146C= MANE Select	ENSP00000373574.4:p.Ala49=
ENST00000388922.8:c.146C=	ENSP00000373574.4:p.Ala49=
ENST00000419526.6:c.103+648C=	ENSP00000392492.2:n.103+648C=
ENST00000547400.5:c.188C=	ENSP00000446724.1:p.Ala63=
ENST00000550683.5:c.188C=	ENSP00000447884.1:p.Ala63=
ENST00000551576.5:c.146C=	ENSP00000455848.1:p.Ala49=
NM_000020.2:c.146C= , LRG_543t1:c.146C=	NP_000011.2:p.Ala49=
NM_001077401.1:c.146C=	NP_001070869.1:p.Ala49=
XM_005269235.2:c.146C=	XP_005269292.1:p.Ala49=
XM_011539008.1:c.188C=	XP_011537310.1:p.Ala63=
NM_000020.3:c.146C= MANE Select	NP_000011.2:p.Ala49=
NM_001077401.2:c.146C=	NP_001070869.1:p.Ala49=