Canonical Allele Identifier: CA384900417

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2001605
• ClinVar RCV Id: RCV002815579
• MyVariant Identifiers: chr12:g.52309048C>G (hg19) ; chr12:g.51915264C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915264C>G , CM000674.2:g.51915264C>G	GRCh38
NC_000012.11:g.52309048C>G , CM000674.1:g.52309048C>G	GRCh37
NC_000012.10:g.50595315C>G	NCBI36
NG_009549.1:g.12847C>G , LRG_543:g.12847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.542C>G	ENSP00000446724.2:p.Thr181Arg
ENST00000551576.6:c.812C>G	ENSP00000455848.2:p.Thr271Arg
ENST00000552678.2:c.812C>G	ENSP00000457394.2:p.Thr271Arg
ENST00000388922.9:c.812C>G MANE Select	ENSP00000373574.4:p.Thr271Arg
ENST00000388922.8:c.812C>G	ENSP00000373574.4:p.Thr271Arg
ENST00000419526.6:c.290C>G	ENSP00000392492.2:p.Thr97Arg
ENST00000550683.5:c.854C>G	ENSP00000447884.1:p.Thr285Arg
NM_000020.2:c.812C>G , LRG_543t1:c.812C>G	NP_000011.2:p.Thr271Arg
NM_001077401.1:c.812C>G	NP_001070869.1:p.Thr271Arg
XM_005269235.2:c.812C>G	XP_005269292.1:p.Thr271Arg
XM_011539008.1:c.542C>G	XP_011537310.1:p.Thr181Arg
XM_024449279.1:c.23C>G	XP_024305047.1:p.Thr8Arg
NM_000020.3:c.812C>G MANE Select	NP_000011.2:p.Thr271Arg
NM_001077401.2:c.812C>G	NP_001070869.1:p.Thr271Arg