Canonical Allele Identifier: CA2036266107
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51912397G= , CM000674.2:g.51912397G= GRCh38
NC_000012.11:g.52306181G= , CM000674.1:g.52306181G= GRCh37
NC_000012.10:g.50592448G= NCBI36
NG_009549.1:g.9980G= , LRG_543:g.9980G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.-36G= ENSP00000446724.2:n.-36G=
ENST00000551576.6:c.-5-73G= ENSP00000455848.2:n.-5-73G=
ENST00000552678.2:c.-5-73G= ENSP00000457394.2:n.-5-73G=
ENST00000388922.9:c.-5-73G= MANE Select ENSP00000373574.4:n.-5-73G=
ENST00000388922.8:c.-5-73G= ENSP00000373574.4:n.-5-73G=
ENST00000419526.6:c.-36G= ENSP00000392492.2:n.-36G=
ENST00000547400.5:c.-36G= ENSP00000446724.1:n.-36G=
ENST00000550683.5:c.-36G= ENSP00000447884.1:n.-36G=
ENST00000551576.5:c.-5-73G= ENSP00000455848.1:n.-5-73G=
NM_000020.2:c.-5-73G= , LRG_543t1:c.-5-73G= NP_000011.2:n.-5-73G=
NM_001077401.1:c.-78G= NP_001070869.1:n.-78G=
XM_005269235.2:c.-5-73G= XP_005269292.1:n.-5-73G=
XM_011539008.1:c.-36G= XP_011537310.1:n.-36G=
NM_000020.3:c.-5-73G= MANE Select NP_000011.2:n.-5-73G=
NM_001077401.2:c.-78G= NP_001070869.1:n.-78G=