Canonical Allele Identifier: CA2036239976
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51919144G= , CM000674.2:g.51919144G= GRCh38
NC_000012.11:g.52312928G= , CM000674.1:g.52312928G= GRCh37
NC_000012.10:g.50599195G= NCBI36
NG_009549.1:g.16727G= , LRG_543:g.16727G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.1107+29G= ENSP00000446724.2:n.1107+29G=
ENST00000551576.6:c.1377+29G= ENSP00000455848.2:n.1377+29G=
ENST00000552678.2:c.1406G= ENSP00000457394.2:p.Arg469=
ENST00000388922.9:c.1377+29G= MANE Select ENSP00000373574.4:n.1377+29G=
ENST00000388922.8:c.1377+29G= ENSP00000373574.4:n.1377+29G=
ENST00000419526.6:c.855+29G= ENSP00000392492.2:n.855+29G=
ENST00000547632.1:n.681G=
ENST00000550683.5:c.1419+29G= ENSP00000447884.1:n.1419+29G=
ENST00000552678.1:c.411G=
NM_000020.2:c.1377+29G= , LRG_543t1:c.1377+29G= NP_000011.2:n.1377+29G=
NM_001077401.1:c.1377+29G= NP_001070869.1:n.1377+29G=
XM_005269235.2:c.1377+29G= XP_005269292.1:n.1377+29G=
XM_011539008.1:c.1107+29G= XP_011537310.1:n.1107+29G=
XM_024449279.1:c.588+29G= XP_024305047.1:n.588+29G=
NM_000020.3:c.1377+29G= MANE Select NP_000011.2:n.1377+29G=
NM_001077401.2:c.1377+29G= NP_001070869.1:n.1377+29G=