Canonical Allele Identifier: CA2580086421
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1752360
ClinVar RCV Id: RCV002366593

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913063_51913103delinsTGAAG , CM000674.2:g.51913063_51913103delinsTGAAG GRCh38
NC_000012.11:g.52306847_52306887delinsTGAAG , CM000674.1:g.52306847_52306887delinsTGAAG GRCh37
NC_000012.10:g.50593114_50593154delinsTGAAG NCBI36
NG_009549.1:g.10646_10686delinsTGAAG , LRG_543:g.10646_10686delinsTGAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.104-36_108delinsTGAAG
ENST00000551576.6:c.62-36_66delinsTGAAG
ENST00000552678.2:c.62-36_66delinsTGAAG
ENST00000388922.9:c.62-36_66delinsTGAAG
ENST00000388922.8:c.62-36_66delinsTGAAG
ENST00000419526.6:c.103+528_103+568delinsTGAAG ENSP00000392492.2:n.103+528_103+568delins...
ENST00000547400.5:c.104-36_108delinsTGAAG
ENST00000550683.5:c.104-36_108delinsTGAAG
ENST00000551576.5:c.62-36_66delinsTGAAG
NM_000020.2:c.62-36_66delinsTGAAG , LRG_543t1:c.62-36_66delinsTGAAG
NM_001077401.1:c.62-36_66delinsTGAAG
XM_005269235.2:c.62-36_66delinsTGAAG
XM_011539008.1:c.104-36_108delinsTGAAG
NM_000020.3:c.62-36_66delinsTGAAG
NM_001077401.2:c.62-36_66delinsTGAAG