Canonical Allele Identifier: CA321832
Gene: ACVRL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212801
dbSNP Id: rs863223412

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915438G>A , CM000674.2:g.51915438G>A GRCh38
NC_000012.11:g.52309222G>A , CM000674.1:g.52309222G>A GRCh37
NC_000012.10:g.50595489G>A NCBI36
NG_009549.1:g.13021G>A , LRG_543:g.13021G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.716G>A ENSP00000446724.2:p.Arg239His
ENST00000551576.6:c.986G>A ENSP00000455848.2:p.Arg329His
ENST00000552678.2:c.986G>A ENSP00000457394.2:p.Arg329His
ENST00000388922.9:c.986G>A MANE Select ENSP00000373574.4:p.Arg329His
ENST00000388922.8:c.986G>A ENSP00000373574.4:p.Arg329His
ENST00000419526.6:c.464G>A ENSP00000392492.2:p.Arg155His
ENST00000550683.5:c.1028G>A ENSP00000447884.1:p.Arg343His
NM_000020.2:c.986G>A , LRG_543t1:c.986G>A NP_000011.2:p.Arg329His
NM_001077401.1:c.986G>A NP_001070869.1:p.Arg329His
XM_005269235.2:c.986G>A XP_005269292.1:p.Arg329His
XM_011539008.1:c.716G>A XP_011537310.1:p.Arg239His
XM_024449279.1:c.197G>A XP_024305047.1:p.Arg66His
NM_000020.3:c.986G>A MANE Select NP_000011.2:p.Arg329His
NM_001077401.2:c.986G>A NP_001070869.1:p.Arg329His