Canonical Allele Identifier: CA480063162

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52309064C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915280C>A , CM000674.2:g.51915280C>A	GRCh38
NC_000012.11:g.52309064C>A , CM000674.1:g.52309064C>A	GRCh37
NC_000012.10:g.50595331C>A	NCBI36
NG_009549.1:g.12863C>A , LRG_543:g.12863C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.558C>A	ENSP00000446724.2:p.Ile186=
ENST00000551576.6:c.828C>A	ENSP00000455848.2:p.Ile276=
ENST00000552678.2:c.828C>A	ENSP00000457394.2:p.Ile276=
ENST00000388922.9:c.828C>A MANE Select	ENSP00000373574.4:p.Ile276=
ENST00000388922.8:c.828C>A	ENSP00000373574.4:p.Ile276=
ENST00000419526.6:c.306C>A	ENSP00000392492.2:p.Ile102=
ENST00000550683.5:c.870C>A	ENSP00000447884.1:p.Ile290=
NM_000020.2:c.828C>A , LRG_543t1:c.828C>A	NP_000011.2:p.Ile276=
NM_001077401.1:c.828C>A	NP_001070869.1:p.Ile276=
XM_005269235.2:c.828C>A	XP_005269292.1:p.Ile276=
XM_011539008.1:c.558C>A	XP_011537310.1:p.Ile186=
XM_024449279.1:c.39C>A	XP_024305047.1:p.Ile13=
NM_000020.3:c.828C>A MANE Select	NP_000011.2:p.Ile276=
NM_001077401.2:c.828C>A	NP_001070869.1:p.Ile276=