Canonical Allele Identifier: CA2036236375

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915637A= , CM000674.2:g.51915637A=	GRCh38
NC_000012.11:g.52309421A= , CM000674.1:g.52309421A=	GRCh37
NC_000012.10:g.50595688A=	NCBI36
NG_009549.1:g.13220A= , LRG_543:g.13220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.778+137A=	ENSP00000446724.2:n.778+137A=
ENST00000551576.6:c.1048+137A=	ENSP00000455848.2:n.1048+137A=
ENST00000552678.2:c.1048+137A=	ENSP00000457394.2:n.1048+137A=
ENST00000388922.9:c.1048+137A= MANE Select	ENSP00000373574.4:n.1048+137A=
ENST00000388922.8:c.1048+137A=	ENSP00000373574.4:n.1048+137A=
ENST00000419526.6:c.526+137A=	ENSP00000392492.2:n.526+137A=
ENST00000550683.5:c.1090+137A=	ENSP00000447884.1:n.1090+137A=
ENST00000552678.1:c.53+137A=
NM_000020.2:c.1048+137A= , LRG_543t1:c.1048+137A=	NP_000011.2:n.1048+137A=
NM_001077401.1:c.1048+137A=	NP_001070869.1:n.1048+137A=
XM_005269235.2:c.1048+137A=	XP_005269292.1:n.1048+137A=
XM_011539008.1:c.778+137A=	XP_011537310.1:n.778+137A=
XM_024449279.1:c.259+137A=	XP_024305047.1:n.259+137A=
NM_000020.3:c.1048+137A= MANE Select	NP_000011.2:n.1048+137A=
NM_001077401.2:c.1048+137A=	NP_001070869.1:n.1048+137A=