Canonical Allele Identifier: CA916081669
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 836378
ClinVar RCV Id: RCV001037493
dbSNP Id: rs1940812948

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915482_51915518del , CM000674.2:g.51915482_51915518del GRCh38
NC_000012.11:g.52309266_52309302del , CM000674.1:g.52309266_52309302del GRCh37
NC_000012.10:g.50595533_50595569del NCBI36
NG_009549.1:g.13065_13101del , LRG_543:g.13065_13101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.760_778+18del
ENST00000551576.6:c.1030_1048+18del
ENST00000552678.2:c.1030_1048+18del
ENST00000388922.9:c.1030_1048+18del
ENST00000388922.8:c.1030_1048+18del
ENST00000419526.6:c.508_526+18del
ENST00000550683.5:c.1072_1090+18del
ENST00000552678.1:c.35_53+18del
NM_000020.2:c.1030_1048+18del , LRG_543t1:c.1030_1048+18del
NM_001077401.1:c.1030_1048+18del
XM_005269235.2:c.1030_1048+18del
XM_011539008.1:c.760_778+18del
XM_024449279.1:c.241_259+18del
NM_000020.3:c.1030_1048+18del
NM_001077401.2:c.1030_1048+18del