Canonical Allele Identifier: CA2036266186
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51912446C= , CM000674.2:g.51912446C= GRCh38
NC_000012.11:g.52306230C= , CM000674.1:g.52306230C= GRCh37
NC_000012.10:g.50592497C= NCBI36
NG_009549.1:g.10029C= , LRG_543:g.10029C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.14C= ENSP00000446724.2:p.Pro5=
ENST00000551576.6:c.-5-24C= ENSP00000455848.2:n.-5-24C=
ENST00000552678.2:c.-5-24C= ENSP00000457394.2:n.-5-24C=
ENST00000388922.9:c.-5-24C= MANE Select ENSP00000373574.4:n.-5-24C=
ENST00000388922.8:c.-5-24C= ENSP00000373574.4:n.-5-24C=
ENST00000419526.6:c.14C= ENSP00000392492.2:p.Pro5=
ENST00000547400.5:c.14C= ENSP00000446724.1:p.Pro5=
ENST00000550683.5:c.14C= ENSP00000447884.1:p.Pro5=
ENST00000551576.5:c.-5-24C= ENSP00000455848.1:n.-5-24C=
NM_000020.2:c.-5-24C= , LRG_543t1:c.-5-24C= NP_000011.2:n.-5-24C=
NM_001077401.1:c.-29C= NP_001070869.1:n.-29C=
XM_005269235.2:c.-5-24C= XP_005269292.1:n.-5-24C=
XM_011539008.1:c.14C= XP_011537310.1:p.Pro5=
NM_000020.3:c.-5-24C= MANE Select NP_000011.2:n.-5-24C=
NM_001077401.2:c.-29C= NP_001070869.1:n.-29C=