Canonical Allele Identifier: CA2842605621
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913154del , CM000674.2:g.51913154del GRCh38
NC_000012.11:g.52306938del , CM000674.1:g.52306938del GRCh37
NC_000012.10:g.50593205del NCBI36
NG_009549.1:g.10737del , LRG_543:g.10737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.159del ENSP00000446724.2:p.His54IlefsTer14
ENST00000551576.6:c.117del ENSP00000455848.2:p.His40IlefsTer14
ENST00000552678.2:c.117del ENSP00000457394.2:p.His40IlefsTer14
ENST00000388922.9:c.117del MANE Select ENSP00000373574.4:p.His40IlefsTer14
ENST00000388922.8:c.117del ENSP00000373574.4:p.His40IlefsTer14
ENST00000419526.6:c.103+619del ENSP00000392492.2:n.103+619del
ENST00000547400.5:c.159del ENSP00000446724.1:p.His54IlefsTer14
ENST00000550683.5:c.159del ENSP00000447884.1:p.His54IlefsTer14
ENST00000551576.5:c.117del ENSP00000455848.1:p.His40IlefsTer14
NM_000020.2:c.117del , LRG_543t1:c.117del NP_000011.2:p.His40IlefsTer14
NM_001077401.1:c.117del NP_001070869.1:p.His40IlefsTer14
XM_005269235.2:c.117del XP_005269292.1:p.His40IlefsTer14
XM_011539008.1:c.159del XP_011537310.1:p.His54IlefsTer14
NM_000020.3:c.117del MANE Select NP_000011.2:p.His40IlefsTer14
NM_001077401.2:c.117del NP_001070869.1:p.His40IlefsTer14