Canonical Allele Identifier: CA384897742
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913192C>A , CM000674.2:g.51913192C>A GRCh38
NC_000012.11:g.52306976C>A , CM000674.1:g.52306976C>A GRCh37
NC_000012.10:g.50593243C>A NCBI36
NG_009549.1:g.10775C>A , LRG_543:g.10775C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.197C>A ENSP00000446724.2:p.Thr66Lys
ENST00000551576.6:c.155C>A ENSP00000455848.2:p.Thr52Lys
ENST00000552678.2:c.155C>A ENSP00000457394.2:p.Thr52Lys
ENST00000388922.9:c.155C>A MANE Select ENSP00000373574.4:p.Thr52Lys
ENST00000388922.8:c.155C>A ENSP00000373574.4:p.Thr52Lys
ENST00000419526.6:c.103+657C>A ENSP00000392492.2:n.103+657C>A
ENST00000547400.5:c.197C>A ENSP00000446724.1:p.Thr66Lys
ENST00000550683.5:c.197C>A ENSP00000447884.1:p.Thr66Lys
ENST00000551576.5:c.155C>A ENSP00000455848.1:p.Thr52Lys
NM_000020.2:c.155C>A , LRG_543t1:c.155C>A NP_000011.2:p.Thr52Lys
NM_001077401.1:c.155C>A NP_001070869.1:p.Thr52Lys
XM_005269235.2:c.155C>A XP_005269292.1:p.Thr52Lys
XM_011539008.1:c.197C>A XP_011537310.1:p.Thr66Lys
NM_000020.3:c.155C>A MANE Select NP_000011.2:p.Thr52Lys
NM_001077401.2:c.155C>A NP_001070869.1:p.Thr52Lys