Canonical Allele Identifier: CA658656303
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 464767
ClinVar RCV Id: RCV000528230
dbSNP Id: rs1555152815

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914074del , CM000674.2:g.51914074del GRCh38
NC_000012.11:g.52307858del , CM000674.1:g.52307858del GRCh37
NC_000012.10:g.50594125del NCBI36
NG_009549.1:g.11657del , LRG_543:g.11657del

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-365del ENSP00000446724.2:n.356-365del
ENST00000551576.6:c.625+1del
ENST00000552678.2:c.625+1del
ENST00000388922.9:c.625+1del
ENST00000388922.8:c.625+1del
ENST00000419526.6:c.104-365del ENSP00000392492.2:n.104-365del
ENST00000547400.5:c.356-365del ENSP00000446724.1:n.356-365del
ENST00000550683.5:c.667+1del
NM_000020.2:c.625+1del , LRG_543t1:c.625+1del
NM_001077401.1:c.625+1del
XM_005269235.2:c.625+1del
XM_011539008.1:c.356-365del XP_011537310.1:n.356-365del
XM_024449279.1:c.-165+304del XP_024305047.1:n.-165+304del
NM_000020.3:c.625+1del
NM_001077401.2:c.625+1del