Canonical Allele Identifier: CA2036236612
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915928A= , CM000674.2:g.51915928A= GRCh38
NC_000012.11:g.52309712A= , CM000674.1:g.52309712A= GRCh37
NC_000012.10:g.50595979A= NCBI36
NG_009549.1:g.13511A= , LRG_543:g.13511A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.779-108A= ENSP00000446724.2:n.779-108A=
ENST00000551576.6:c.1049-108A= ENSP00000455848.2:n.1049-108A=
ENST00000552678.2:c.1049-108A= ENSP00000457394.2:n.1049-108A=
ENST00000388922.9:c.1049-108A= MANE Select ENSP00000373574.4:n.1049-108A=
ENST00000388922.8:c.1049-108A= ENSP00000373574.4:n.1049-108A=
ENST00000419526.6:c.527-108A= ENSP00000392492.2:n.527-108A=
ENST00000547632.1:n.216A=
ENST00000550683.5:c.1091-108A= ENSP00000447884.1:n.1091-108A=
ENST00000552678.1:c.54-108A=
NM_000020.2:c.1049-108A= , LRG_543t1:c.1049-108A= NP_000011.2:n.1049-108A=
NM_001077401.1:c.1049-108A= NP_001070869.1:n.1049-108A=
XM_005269235.2:c.1049-108A= XP_005269292.1:n.1049-108A=
XM_011539008.1:c.779-108A= XP_011537310.1:n.779-108A=
XM_024449279.1:c.260-108A= XP_024305047.1:n.260-108A=
NM_000020.3:c.1049-108A= MANE Select NP_000011.2:n.1049-108A=
NM_001077401.2:c.1049-108A= NP_001070869.1:n.1049-108A=