Canonical Allele Identifier: CA384897713

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2132509
• ClinVar RCV Id: RCV003036774
• MyVariant Identifiers: chr12:g.52306972T>A (hg19) ; chr12:g.51913188T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913188T>A , CM000674.2:g.51913188T>A	GRCh38
NC_000012.11:g.52306972T>A , CM000674.1:g.52306972T>A	GRCh37
NC_000012.10:g.50593239T>A	NCBI36
NG_009549.1:g.10771T>A , LRG_543:g.10771T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.193T>A	ENSP00000446724.2:p.Cys65Ser
ENST00000551576.6:c.151T>A	ENSP00000455848.2:p.Cys51Ser
ENST00000552678.2:c.151T>A	ENSP00000457394.2:p.Cys51Ser
ENST00000388922.9:c.151T>A MANE Select	ENSP00000373574.4:p.Cys51Ser
ENST00000388922.8:c.151T>A	ENSP00000373574.4:p.Cys51Ser
ENST00000419526.6:c.103+653T>A	ENSP00000392492.2:n.103+653T>A
ENST00000547400.5:c.193T>A	ENSP00000446724.1:p.Cys65Ser
ENST00000550683.5:c.193T>A	ENSP00000447884.1:p.Cys65Ser
ENST00000551576.5:c.151T>A	ENSP00000455848.1:p.Cys51Ser
NM_000020.2:c.151T>A , LRG_543t1:c.151T>A	NP_000011.2:p.Cys51Ser
NM_001077401.1:c.151T>A	NP_001070869.1:p.Cys51Ser
XM_005269235.2:c.151T>A	XP_005269292.1:p.Cys51Ser
XM_011539008.1:c.193T>A	XP_011537310.1:p.Cys65Ser
NM_000020.3:c.151T>A MANE Select	NP_000011.2:p.Cys51Ser
NM_001077401.2:c.151T>A	NP_001070869.1:p.Cys51Ser