Canonical Allele Identifier: CA2036241828
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920817G= , CM000674.2:g.51920817G= GRCh38
NC_000012.11:g.52314601G= , CM000674.1:g.52314601G= GRCh37
NC_000012.10:g.50600868G= NCBI36
NG_009549.1:g.18400G= , LRG_543:g.18400G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.1166G= ENSP00000446724.2:p.Arg389=
ENST00000551576.6:c.1436G= ENSP00000455848.2:p.Arg479=
ENST00000388922.9:c.1436G= MANE Select ENSP00000373574.4:p.Arg479=
ENST00000388922.8:c.1436G= ENSP00000373574.4:p.Arg479=
ENST00000419526.6:c.914G= ENSP00000392492.2:p.Arg305=
ENST00000550683.5:c.1478G= ENSP00000447884.1:p.Arg493=
NM_000020.2:c.1436G= , LRG_543t1:c.1436G= NP_000011.2:p.Arg479=
NM_001077401.1:c.1436G= NP_001070869.1:p.Arg479=
XM_005269235.2:c.1436G= XP_005269292.1:p.Arg479=
XM_011539008.1:c.1166G= XP_011537310.1:p.Arg389=
XM_024449279.1:c.647G= XP_024305047.1:p.Arg216=
NM_000020.3:c.1436G= MANE Select NP_000011.2:p.Arg479=
NM_001077401.2:c.1436G= NP_001070869.1:p.Arg479=