Canonical Allele Identifier: CA2697559267

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2764965
• ClinVar RCV Id: RCV003510243

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913621del , CM000674.2:g.51913621del	GRCh38
NC_000012.11:g.52307405del , CM000674.1:g.52307405del	GRCh37
NC_000012.10:g.50593672del	NCBI36
NG_009549.1:g.11204del , LRG_543:g.11204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+271del	ENSP00000446724.2:n.355+271del
ENST00000551576.6:c.376del	ENSP00000455848.2:p.Val126CysfsTer?
ENST00000552678.2:c.376del	ENSP00000457394.2:p.Val126CysfsTer?
ENST00000388922.9:c.376del MANE Select	ENSP00000373574.4:p.Val126CysfsTer?
ENST00000388922.8:c.376del	ENSP00000373574.4:p.Val126CysfsTer?
ENST00000419526.6:c.104-818del	ENSP00000392492.2:n.104-818del
ENST00000547400.5:c.355+271del	ENSP00000446724.1:n.355+271del
ENST00000550683.5:c.418del	ENSP00000447884.1:p.Val140CysfsTer?
NM_000020.2:c.376del , LRG_543t1:c.376del	NP_000011.2:p.Val126CysfsTer?
NM_001077401.1:c.376del	NP_001070869.1:p.Val126CysfsTer?
XM_005269235.2:c.376del	XP_005269292.1:p.Val126CysfsTer?
XM_011539008.1:c.355+271del	XP_011537310.1:n.355+271del
XM_024449279.1:c.-314del	XP_024305047.1:n.-314del
NM_000020.3:c.376del MANE Select	NP_000011.2:p.Val126CysfsTer?
NM_001077401.2:c.376del	NP_001070869.1:p.Val126CysfsTer?