Canonical Allele Identifier: CA2036236234
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915483G= , CM000674.2:g.51915483G= GRCh38
NC_000012.11:g.52309267G= , CM000674.1:g.52309267G= GRCh37
NC_000012.10:g.50595534G= NCBI36
NG_009549.1:g.13066G= , LRG_543:g.13066G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.761G= ENSP00000446724.2:p.Cys254=
ENST00000551576.6:c.1031G= ENSP00000455848.2:p.Cys344=
ENST00000552678.2:c.1031G= ENSP00000457394.2:p.Cys344=
ENST00000388922.9:c.1031G= MANE Select ENSP00000373574.4:p.Cys344=
ENST00000388922.8:c.1031G= ENSP00000373574.4:p.Cys344=
ENST00000419526.6:c.509G= ENSP00000392492.2:p.Cys170=
ENST00000550683.5:c.1073G= ENSP00000447884.1:p.Cys358=
ENST00000552678.1:c.36G=
NM_000020.2:c.1031G= , LRG_543t1:c.1031G= NP_000011.2:p.Cys344=
NM_001077401.1:c.1031G= NP_001070869.1:p.Cys344=
XM_005269235.2:c.1031G= XP_005269292.1:p.Cys344=
XM_011539008.1:c.761G= XP_011537310.1:p.Cys254=
XM_024449279.1:c.242G= XP_024305047.1:p.Cys81=
NM_000020.3:c.1031G= MANE Select NP_000011.2:p.Cys344=
NM_001077401.2:c.1031G= NP_001070869.1:p.Cys344=