Canonical Allele Identifier: CA1630855699
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914237T= , CM000674.2:g.51914237T= GRCh38
NC_000012.11:g.52308021T= , CM000674.1:g.52308021T= GRCh37
NC_000012.10:g.50594288T= NCBI36
NG_009549.1:g.11820T= , LRG_543:g.11820T=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-202T= ENSP00000446724.2:n.356-202T=
ENST00000551576.6:c.625+164T= ENSP00000455848.2:n.625+164T=
ENST00000552678.2:c.625+164T= ENSP00000457394.2:n.625+164T=
ENST00000388922.9:c.625+164T= MANE Select ENSP00000373574.4:n.625+164T=
ENST00000388922.8:c.625+164T= ENSP00000373574.4:n.625+164T=
ENST00000419526.6:c.104-202T= ENSP00000392492.2:n.104-202T=
ENST00000547400.5:c.356-202T= ENSP00000446724.1:n.356-202T=
ENST00000550683.5:c.667+164T= ENSP00000447884.1:n.667+164T=
NM_000020.2:c.625+164T= , LRG_543t1:c.625+164T= NP_000011.2:n.625+164T=
NM_001077401.1:c.625+164T= NP_001070869.1:n.625+164T=
XM_005269235.2:c.625+164T= XP_005269292.1:n.625+164T=
XM_011539008.1:c.356-202T= XP_011537310.1:n.356-202T=
XM_024449279.1:c.-164-202T= XP_024305047.1:n.-164-202T=
NM_000020.3:c.625+164T= MANE Select NP_000011.2:n.625+164T=
NM_001077401.2:c.625+164T= NP_001070869.1:n.625+164T=