Canonical Allele Identifier: CA913191252

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 617664
• ClinVar RCV Id: RCV000754826
• dbSNP Id: rs111710113

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920543C>G , CM000674.2:g.51920543C>G	GRCh38
NC_000012.11:g.52314327C>G , CM000674.1:g.52314327C>G	GRCh37
NC_000012.10:g.50600594C>G	NCBI36
NG_009549.1:g.18126C>G , LRG_543:g.18126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1108-216C>G	ENSP00000446724.2:n.1108-216C>G
ENST00000551576.6:c.1378-216C>G	ENSP00000455848.2:n.1378-216C>G
ENST00000388922.9:c.1378-216C>G MANE Select	ENSP00000373574.4:n.1378-216C>G
ENST00000388922.8:c.1378-216C>G	ENSP00000373574.4:n.1378-216C>G
ENST00000419526.6:c.856-216C>G	ENSP00000392492.2:n.856-216C>G
ENST00000550683.5:c.1420-216C>G	ENSP00000447884.1:n.1420-216C>G
NM_000020.2:c.1378-216C>G , LRG_543t1:c.1378-216C>G	NP_000011.2:n.1378-216C>G
NM_001077401.1:c.1378-216C>G	NP_001070869.1:n.1378-216C>G
XM_005269235.2:c.1378-216C>G	XP_005269292.1:n.1378-216C>G
XM_011539008.1:c.1108-216C>G	XP_011537310.1:n.1108-216C>G
XM_024449279.1:c.589-216C>G	XP_024305047.1:n.589-216C>G
NM_000020.3:c.1378-216C>G MANE Select	NP_000011.2:n.1378-216C>G
NM_001077401.2:c.1378-216C>G	NP_001070869.1:n.1378-216C>G