Canonical Allele Identifier: CA384901069

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52309164C>A (hg19) ; chr12:g.51915380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915380C>A , CM000674.2:g.51915380C>A	GRCh38
NC_000012.11:g.52309164C>A , CM000674.1:g.52309164C>A	GRCh37
NC_000012.10:g.50595431C>A	NCBI36
NG_009549.1:g.12963C>A , LRG_543:g.12963C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.658C>A	ENSP00000446724.2:p.Leu220Met
ENST00000551576.6:c.928C>A	ENSP00000455848.2:p.Leu310Met
ENST00000552678.2:c.928C>A	ENSP00000457394.2:p.Leu310Met
ENST00000388922.9:c.928C>A MANE Select	ENSP00000373574.4:p.Leu310Met
ENST00000388922.8:c.928C>A	ENSP00000373574.4:p.Leu310Met
ENST00000419526.6:c.406C>A	ENSP00000392492.2:p.Leu136Met
ENST00000550683.5:c.970C>A	ENSP00000447884.1:p.Leu324Met
NM_000020.2:c.928C>A , LRG_543t1:c.928C>A	NP_000011.2:p.Leu310Met
NM_001077401.1:c.928C>A	NP_001070869.1:p.Leu310Met
XM_005269235.2:c.928C>A	XP_005269292.1:p.Leu310Met
XM_011539008.1:c.658C>A	XP_011537310.1:p.Leu220Met
XM_024449279.1:c.139C>A	XP_024305047.1:p.Leu47Met
NM_000020.3:c.928C>A MANE Select	NP_000011.2:p.Leu310Met
NM_001077401.2:c.928C>A	NP_001070869.1:p.Leu310Met