Canonical Allele Identifier: CA2580086423

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1757184
• ClinVar RCV Id: RCV002367369

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913108_51913130del , CM000674.2:g.51913108_51913130del	GRCh38
NC_000012.11:g.52306892_52306914del , CM000674.1:g.52306892_52306914del	GRCh37
NC_000012.10:g.50593159_50593181del	NCBI36
NG_009549.1:g.10691_10713del , LRG_543:g.10691_10713del

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.113_135del	ENSP00000446724.2:p.Val38GlyfsTer6
ENST00000551576.6:c.71_93del	ENSP00000455848.2:p.Val24GlyfsTer6
ENST00000552678.2:c.71_93del	ENSP00000457394.2:p.Val24GlyfsTer6
ENST00000388922.9:c.71_93del MANE Select	ENSP00000373574.4:p.Val24GlyfsTer6
ENST00000388922.8:c.71_93del	ENSP00000373574.4:p.Val24GlyfsTer6
ENST00000419526.6:c.103+573_103+595del	ENSP00000392492.2:n.103+573_103+595del
ENST00000547400.5:c.113_135del	ENSP00000446724.1:p.Val38GlyfsTer6
ENST00000550683.5:c.113_135del	ENSP00000447884.1:p.Val38GlyfsTer6
ENST00000551576.5:c.71_93del	ENSP00000455848.1:p.Val24GlyfsTer6
NM_000020.2:c.71_93del , LRG_543t1:c.71_93del	NP_000011.2:p.Val24GlyfsTer6
NM_001077401.1:c.71_93del	NP_001070869.1:p.Val24GlyfsTer6
XM_005269235.2:c.71_93del	XP_005269292.1:p.Val24GlyfsTer6
XM_011539008.1:c.113_135del	XP_011537310.1:p.Val38GlyfsTer6
NM_000020.3:c.71_93del MANE Select	NP_000011.2:p.Val24GlyfsTer6
NM_001077401.2:c.71_93del	NP_001070869.1:p.Val24GlyfsTer6