Canonical Allele Identifier: CA2580086429
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767713
ClinVar RCV Id: RCV002376523

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913165_51913169del , CM000674.2:g.51913165_51913169del GRCh38
NC_000012.11:g.52306949_52306953del , CM000674.1:g.52306949_52306953del GRCh37
NC_000012.10:g.50593216_50593220del NCBI36
NG_009549.1:g.10748_10752del , LRG_543:g.10748_10752del

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.170_174del ENSP00000446724.2:p.Gly57AspfsTer?
ENST00000551576.6:c.128_132del ENSP00000455848.2:p.Gly43AspfsTer?
ENST00000552678.2:c.128_132del ENSP00000457394.2:p.Gly43AspfsTer?
ENST00000388922.9:c.128_132del MANE Select ENSP00000373574.4:p.Gly43AspfsTer?
ENST00000388922.8:c.128_132del ENSP00000373574.4:p.Gly43AspfsTer?
ENST00000419526.6:c.103+630_103+634del ENSP00000392492.2:n.103+630_103+634del
ENST00000547400.5:c.170_174del ENSP00000446724.1:p.Gly57AspfsTer?
ENST00000550683.5:c.170_174del ENSP00000447884.1:p.Gly57AspfsTer?
ENST00000551576.5:c.128_132del ENSP00000455848.1:p.Gly43AspfsTer?
NM_000020.2:c.128_132del , LRG_543t1:c.128_132del NP_000011.2:p.Gly43AspfsTer?
NM_001077401.1:c.128_132del NP_001070869.1:p.Gly43AspfsTer?
XM_005269235.2:c.128_132del XP_005269292.1:p.Gly43AspfsTer?
XM_011539008.1:c.170_174del XP_011537310.1:p.Gly57AspfsTer?
NM_000020.3:c.128_132del MANE Select NP_000011.2:p.Gly43AspfsTer?
NM_001077401.2:c.128_132del NP_001070869.1:p.Gly43AspfsTer?