Canonical Allele Identifier: CA2580086443
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1727954
ClinVar RCV Id: RCV002320586

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913350_51913351del , CM000674.2:g.51913350_51913351del GRCh38
NC_000012.11:g.52307134_52307135del , CM000674.1:g.52307134_52307135del GRCh37
NC_000012.10:g.50593401_50593402del NCBI36
NG_009549.1:g.10933_10934del , LRG_543:g.10933_10934del

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.355_355+1del
ENST00000551576.6:c.313_313+1del
ENST00000552678.2:c.313_313+1del
ENST00000388922.9:c.313_313+1del
ENST00000388922.8:c.313_313+1del
ENST00000419526.6:c.103+815_103+816del ENSP00000392492.2:n.103+815_103+816del
ENST00000547400.5:c.355_355+1del
ENST00000550683.5:c.355_355+1del
NM_000020.2:c.313_313+1del , LRG_543t1:c.313_313+1del
NM_001077401.1:c.313_313+1del
XM_005269235.2:c.313_313+1del
XM_011539008.1:c.355_355+1del
XM_024449279.1:c.-377_-377+1del
NM_000020.3:c.313_313+1del
NM_001077401.2:c.313_313+1del