Canonical Allele Identifier: CA2573148775
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403776
ClinVar RCV Id: RCV001901303
dbSNP Id: rs2139065347

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913260del , CM000674.2:g.51913260del GRCh38
NC_000012.11:g.52307044del , CM000674.1:g.52307044del GRCh37
NC_000012.10:g.50593311del NCBI36
NG_009549.1:g.10843del , LRG_543:g.10843del

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.265del ENSP00000446724.2:p.Glu89SerfsTer?
ENST00000551576.6:c.223del ENSP00000455848.2:p.Glu75SerfsTer?
ENST00000552678.2:c.223del ENSP00000457394.2:p.Glu75SerfsTer?
ENST00000388922.9:c.223del MANE Select ENSP00000373574.4:p.Glu75SerfsTer?
ENST00000388922.8:c.223del ENSP00000373574.4:p.Glu75SerfsTer?
ENST00000419526.6:c.103+725del ENSP00000392492.2:n.103+725del
ENST00000547400.5:c.265del ENSP00000446724.1:p.Glu89SerfsTer?
ENST00000550683.5:c.265del ENSP00000447884.1:p.Glu89SerfsTer?
ENST00000551576.5:c.223del ENSP00000455848.1:p.Glu75SerfsTer?
NM_000020.2:c.223del , LRG_543t1:c.223del NP_000011.2:p.Glu75SerfsTer?
NM_001077401.1:c.223del NP_001070869.1:p.Glu75SerfsTer?
XM_005269235.2:c.223del XP_005269292.1:p.Glu75SerfsTer?
XM_011539008.1:c.265del XP_011537310.1:p.Glu89SerfsTer?
NM_000020.3:c.223del MANE Select NP_000011.2:p.Glu75SerfsTer?
NM_001077401.2:c.223del NP_001070869.1:p.Glu75SerfsTer?