Canonical Allele Identifier: CA2036237251

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51916273A= , CM000674.2:g.51916273A=	GRCh38
NC_000012.11:g.52310057A= , CM000674.1:g.52310057A=	GRCh37
NC_000012.10:g.50596324A=	NCBI36
NG_009549.1:g.13856A= , LRG_543:g.13856A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.976+40A=	ENSP00000446724.2:n.976+40A=
ENST00000551576.6:c.1246+40A=	ENSP00000455848.2:n.1246+40A=
ENST00000552678.2:c.1246+40A=	ENSP00000457394.2:n.1246+40A=
ENST00000388922.9:c.1246+40A= MANE Select	ENSP00000373574.4:n.1246+40A=
ENST00000388922.8:c.1246+40A=	ENSP00000373574.4:n.1246+40A=
ENST00000419526.6:c.724+40A=	ENSP00000392492.2:n.724+40A=
ENST00000547632.1:n.521+40A=
ENST00000550683.5:c.1288+40A=	ENSP00000447884.1:n.1288+40A=
ENST00000552678.1:c.251+40A=
NM_000020.2:c.1246+40A= , LRG_543t1:c.1246+40A=	NP_000011.2:n.1246+40A=
NM_001077401.1:c.1246+40A=	NP_001070869.1:n.1246+40A=
XM_005269235.2:c.1246+40A=	XP_005269292.1:n.1246+40A=
XM_011539008.1:c.976+40A=	XP_011537310.1:n.976+40A=
XM_024449279.1:c.457+40A=	XP_024305047.1:n.457+40A=
NM_000020.3:c.1246+40A= MANE Select	NP_000011.2:n.1246+40A=
NM_001077401.2:c.1246+40A=	NP_001070869.1:n.1246+40A=