Canonical Allele Identifier: CA2036239644

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51918978T= , CM000674.2:g.51918978T=	GRCh38
NC_000012.11:g.52312762T= , CM000674.1:g.52312762T=	GRCh37
NC_000012.10:g.50599029T=	NCBI36
NG_009549.1:g.16561T= , LRG_543:g.16561T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.977-7T=	ENSP00000446724.2:n.977-7T=
ENST00000551576.6:c.1247-7T=	ENSP00000455848.2:n.1247-7T=
ENST00000552678.2:c.1247-7T=	ENSP00000457394.2:n.1247-7T=
ENST00000388922.9:c.1247-7T= MANE Select	ENSP00000373574.4:n.1247-7T=
ENST00000388922.8:c.1247-7T=	ENSP00000373574.4:n.1247-7T=
ENST00000419526.6:c.725-7T=	ENSP00000392492.2:n.725-7T=
ENST00000547632.1:n.522-7T=
ENST00000550683.5:c.1289-7T=	ENSP00000447884.1:n.1289-7T=
ENST00000552678.1:c.252-7T=
NM_000020.2:c.1247-7T= , LRG_543t1:c.1247-7T=	NP_000011.2:n.1247-7T=
NM_001077401.1:c.1247-7T=	NP_001070869.1:n.1247-7T=
XM_005269235.2:c.1247-7T=	XP_005269292.1:n.1247-7T=
XM_011539008.1:c.977-7T=	XP_011537310.1:n.977-7T=
XM_024449279.1:c.458-7T=	XP_024305047.1:n.458-7T=
NM_000020.3:c.1247-7T= MANE Select	NP_000011.2:n.1247-7T=
NM_001077401.2:c.1247-7T=	NP_001070869.1:n.1247-7T=