Canonical Allele Identifier: CA2739272040
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913236del , CM000674.2:g.51913236del GRCh38
NC_000012.11:g.52307020del , CM000674.1:g.52307020del GRCh37
NC_000012.10:g.50593287del NCBI36
NG_009549.1:g.10819del , LRG_543:g.10819del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.241del ENSP00000446724.2:p.Arg81GlyfsTer?
ENST00000551576.6:c.199del ENSP00000455848.2:p.Arg67GlyfsTer?
ENST00000552678.2:c.199del ENSP00000457394.2:p.Arg67GlyfsTer?
ENST00000388922.9:c.199del MANE Select ENSP00000373574.4:p.Arg67GlyfsTer?
ENST00000388922.8:c.199del ENSP00000373574.4:p.Arg67GlyfsTer?
ENST00000419526.6:c.103+701del ENSP00000392492.2:n.103+701del
ENST00000547400.5:c.241del ENSP00000446724.1:p.Arg81GlyfsTer?
ENST00000550683.5:c.241del ENSP00000447884.1:p.Arg81GlyfsTer?
ENST00000551576.5:c.199del ENSP00000455848.1:p.Arg67GlyfsTer?
NM_000020.2:c.199del , LRG_543t1:c.199del NP_000011.2:p.Arg67GlyfsTer?
NM_001077401.1:c.199del NP_001070869.1:p.Arg67GlyfsTer?
XM_005269235.2:c.199del XP_005269292.1:p.Arg67GlyfsTer?
XM_011539008.1:c.241del XP_011537310.1:p.Arg81GlyfsTer?
NM_000020.3:c.199del MANE Select NP_000011.2:p.Arg67GlyfsTer?
NM_001077401.2:c.199del NP_001070869.1:p.Arg67GlyfsTer?