Canonical Allele Identifier: CA480063206

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1765570
• ClinVar RCV Id: RCV002378470
• MyVariant Identifiers: chr12:g.52309139G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915355G>A , CM000674.2:g.51915355G>A	GRCh38
NC_000012.11:g.52309139G>A , CM000674.1:g.52309139G>A	GRCh37
NC_000012.10:g.50595406G>A	NCBI36
NG_009549.1:g.12938G>A , LRG_543:g.12938G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.633G>A	ENSP00000446724.2:p.Arg211=
ENST00000551576.6:c.903G>A	ENSP00000455848.2:p.Arg301=
ENST00000552678.2:c.903G>A	ENSP00000457394.2:p.Arg301=
ENST00000388922.9:c.903G>A MANE Select	ENSP00000373574.4:p.Arg301=
ENST00000388922.8:c.903G>A	ENSP00000373574.4:p.Arg301=
ENST00000419526.6:c.381G>A	ENSP00000392492.2:p.Arg127=
ENST00000550683.5:c.945G>A	ENSP00000447884.1:p.Arg315=
NM_000020.2:c.903G>A , LRG_543t1:c.903G>A	NP_000011.2:p.Arg301=
NM_001077401.1:c.903G>A	NP_001070869.1:p.Arg301=
XM_005269235.2:c.903G>A	XP_005269292.1:p.Arg301=
XM_011539008.1:c.633G>A	XP_011537310.1:p.Arg211=
XM_024449279.1:c.114G>A	XP_024305047.1:p.Arg38=
NM_000020.3:c.903G>A MANE Select	NP_000011.2:p.Arg301=
NM_001077401.2:c.903G>A	NP_001070869.1:p.Arg301=