Canonical Allele Identifier: CA384897899
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913243G>C , CM000674.2:g.51913243G>C GRCh38
NC_000012.11:g.52307027G>C , CM000674.1:g.52307027G>C GRCh37
NC_000012.10:g.50593294G>C NCBI36
NG_009549.1:g.10826G>C , LRG_543:g.10826G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.248G>C ENSP00000446724.2:p.Cys83Ser
ENST00000551576.6:c.206G>C ENSP00000455848.2:p.Cys69Ser
ENST00000552678.2:c.206G>C ENSP00000457394.2:p.Cys69Ser
ENST00000388922.9:c.206G>C MANE Select ENSP00000373574.4:p.Cys69Ser
ENST00000388922.8:c.206G>C ENSP00000373574.4:p.Cys69Ser
ENST00000419526.6:c.103+708G>C ENSP00000392492.2:n.103+708G>C
ENST00000547400.5:c.248G>C ENSP00000446724.1:p.Cys83Ser
ENST00000550683.5:c.248G>C ENSP00000447884.1:p.Cys83Ser
ENST00000551576.5:c.206G>C ENSP00000455848.1:p.Cys69Ser
NM_000020.2:c.206G>C , LRG_543t1:c.206G>C NP_000011.2:p.Cys69Ser
NM_001077401.1:c.206G>C NP_001070869.1:p.Cys69Ser
XM_005269235.2:c.206G>C XP_005269292.1:p.Cys69Ser
XM_011539008.1:c.248G>C XP_011537310.1:p.Cys83Ser
NM_000020.3:c.206G>C MANE Select NP_000011.2:p.Cys69Ser
NM_001077401.2:c.206G>C NP_001070869.1:p.Cys69Ser