Canonical Allele Identifier: CA2036237024
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51916153G= , CM000674.2:g.51916153G= GRCh38
NC_000012.11:g.52309937G= , CM000674.1:g.52309937G= GRCh37
NC_000012.10:g.50596204G= NCBI36
NG_009549.1:g.13736G= , LRG_543:g.13736G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.896G= ENSP00000446724.2:p.Cys299=
ENST00000551576.6:c.1166G= ENSP00000455848.2:p.Cys389=
ENST00000552678.2:c.1166G= ENSP00000457394.2:p.Cys389=
ENST00000388922.9:c.1166G= MANE Select ENSP00000373574.4:p.Cys389=
ENST00000388922.8:c.1166G= ENSP00000373574.4:p.Cys389=
ENST00000419526.6:c.644G= ENSP00000392492.2:p.Cys215=
ENST00000547632.1:n.441G=
ENST00000550683.5:c.1208G= ENSP00000447884.1:p.Cys403=
ENST00000552678.1:c.171G=
NM_000020.2:c.1166G= , LRG_543t1:c.1166G= NP_000011.2:p.Cys389=
NM_001077401.1:c.1166G= NP_001070869.1:p.Cys389=
XM_005269235.2:c.1166G= XP_005269292.1:p.Cys389=
XM_011539008.1:c.896G= XP_011537310.1:p.Cys299=
XM_024449279.1:c.377G= XP_024305047.1:p.Cys126=
NM_000020.3:c.1166G= MANE Select NP_000011.2:p.Cys389=
NM_001077401.2:c.1166G= NP_001070869.1:p.Cys389=