Canonical Allele Identifier: CA2036266735

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913028C= , CM000674.2:g.51913028C=	GRCh38
NC_000012.11:g.52306812C= , CM000674.1:g.52306812C=	GRCh37
NC_000012.10:g.50593079C=	NCBI36
NG_009549.1:g.10611C= , LRG_543:g.10611C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.104-71C=	ENSP00000446724.2:n.104-71C=
ENST00000551576.6:c.62-71C=	ENSP00000455848.2:n.62-71C=
ENST00000552678.2:c.62-71C=	ENSP00000457394.2:n.62-71C=
ENST00000388922.9:c.62-71C= MANE Select	ENSP00000373574.4:n.62-71C=
ENST00000388922.8:c.62-71C=	ENSP00000373574.4:n.62-71C=
ENST00000419526.6:c.103+493C=	ENSP00000392492.2:n.103+493C=
ENST00000547400.5:c.104-71C=	ENSP00000446724.1:n.104-71C=
ENST00000550683.5:c.104-71C=	ENSP00000447884.1:n.104-71C=
ENST00000551576.5:c.62-71C=	ENSP00000455848.1:n.62-71C=
NM_000020.2:c.62-71C= , LRG_543t1:c.62-71C=	NP_000011.2:n.62-71C=
NM_001077401.1:c.62-71C=	NP_001070869.1:n.62-71C=
XM_005269235.2:c.62-71C=	XP_005269292.1:n.62-71C=
XM_011539008.1:c.104-71C=	XP_011537310.1:n.104-71C=
NM_000020.3:c.62-71C= MANE Select	NP_000011.2:n.62-71C=
NM_001077401.2:c.62-71C=	NP_001070869.1:n.62-71C=