Canonical Allele Identifier: CA2036241910
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920832G= , CM000674.2:g.51920832G= GRCh38
NC_000012.11:g.52314616G= , CM000674.1:g.52314616G= GRCh37
NC_000012.10:g.50600883G= NCBI36
NG_009549.1:g.18415G= , LRG_543:g.18415G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.1181G= ENSP00000446724.2:p.Arg394=
ENST00000551576.6:c.1451G= ENSP00000455848.2:p.Arg484=
ENST00000388922.9:c.1451G= MANE Select ENSP00000373574.4:p.Arg484=
ENST00000388922.8:c.1451G= ENSP00000373574.4:p.Arg484=
ENST00000419526.6:c.929G= ENSP00000392492.2:p.Arg310=
ENST00000550683.5:c.1493G= ENSP00000447884.1:p.Arg498=
NM_000020.2:c.1451G= , LRG_543t1:c.1451G= NP_000011.2:p.Arg484=
NM_001077401.1:c.1451G= NP_001070869.1:p.Arg484=
XM_005269235.2:c.1451G= XP_005269292.1:p.Arg484=
XM_011539008.1:c.1181G= XP_011537310.1:p.Arg394=
XM_024449279.1:c.662G= XP_024305047.1:p.Arg221=
NM_000020.3:c.1451G= MANE Select NP_000011.2:p.Arg484=
NM_001077401.2:c.1451G= NP_001070869.1:p.Arg484=