Canonical Allele Identifier: CA480063103

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51913178-G-T
• COSMIC: COSM337345 ; COSM5141033
• MyVariant Identifiers: chr12:g.52306962G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913178G>T , CM000674.2:g.51913178G>T	GRCh38
NC_000012.11:g.52306962G>T , CM000674.1:g.52306962G>T	GRCh37
NC_000012.10:g.50593229G>T	NCBI36
NG_009549.1:g.10761G>T , LRG_543:g.10761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.183G>T	ENSP00000446724.2:p.Arg61=
ENST00000551576.6:c.141G>T	ENSP00000455848.2:p.Arg47=
ENST00000552678.2:c.141G>T	ENSP00000457394.2:p.Arg47=
ENST00000388922.9:c.141G>T MANE Select	ENSP00000373574.4:p.Arg47=
ENST00000388922.8:c.141G>T	ENSP00000373574.4:p.Arg47=
ENST00000419526.6:c.103+643G>T	ENSP00000392492.2:n.103+643G>T
ENST00000547400.5:c.183G>T	ENSP00000446724.1:p.Arg61=
ENST00000550683.5:c.183G>T	ENSP00000447884.1:p.Arg61=
ENST00000551576.5:c.141G>T	ENSP00000455848.1:p.Arg47=
NM_000020.2:c.141G>T , LRG_543t1:c.141G>T	NP_000011.2:p.Arg47=
NM_001077401.1:c.141G>T	NP_001070869.1:p.Arg47=
XM_005269235.2:c.141G>T	XP_005269292.1:p.Arg47=
XM_011539008.1:c.183G>T	XP_011537310.1:p.Arg61=
NM_000020.3:c.141G>T MANE Select	NP_000011.2:p.Arg47=
NM_001077401.2:c.141G>T	NP_001070869.1:p.Arg47=