Canonical Allele Identifier: CA2036269452
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915303C= , CM000674.2:g.51915303C= GRCh38
NC_000012.11:g.52309087C= , CM000674.1:g.52309087C= GRCh37
NC_000012.10:g.50595354C= NCBI36
NG_009549.1:g.12886C= , LRG_543:g.12886C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.581C= ENSP00000446724.2:p.Ser194=
ENST00000551576.6:c.851C= ENSP00000455848.2:p.Ser284=
ENST00000552678.2:c.851C= ENSP00000457394.2:p.Ser284=
ENST00000388922.9:c.851C= MANE Select ENSP00000373574.4:p.Ser284=
ENST00000388922.8:c.851C= ENSP00000373574.4:p.Ser284=
ENST00000419526.6:c.329C= ENSP00000392492.2:p.Ser110=
ENST00000550683.5:c.893C= ENSP00000447884.1:p.Ser298=
NM_000020.2:c.851C= , LRG_543t1:c.851C= NP_000011.2:p.Ser284=
NM_001077401.1:c.851C= NP_001070869.1:p.Ser284=
XM_005269235.2:c.851C= XP_005269292.1:p.Ser284=
XM_011539008.1:c.581C= XP_011537310.1:p.Ser194=
XM_024449279.1:c.62C= XP_024305047.1:p.Ser21=
NM_000020.3:c.851C= MANE Select NP_000011.2:p.Ser284=
NM_001077401.2:c.851C= NP_001070869.1:p.Ser284=