Canonical Allele Identifier: CA2036266005
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51912335C= , CM000674.2:g.51912335C= GRCh38
NC_000012.11:g.52306119C= , CM000674.1:g.52306119C= GRCh37
NC_000012.10:g.50592386C= NCBI36
NG_009549.1:g.9918C= , LRG_543:g.9918C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.-98C= ENSP00000446724.2:n.-98C=
ENST00000551576.6:c.-5-135C= ENSP00000455848.2:n.-5-135C=
ENST00000552678.2:c.-5-135C= ENSP00000457394.2:n.-5-135C=
ENST00000388922.9:c.-5-135C= MANE Select ENSP00000373574.4:n.-5-135C=
ENST00000388922.8:c.-5-135C= ENSP00000373574.4:n.-5-135C=
ENST00000547400.5:c.-98C= ENSP00000446724.1:n.-98C=
ENST00000550683.5:c.-98C= ENSP00000447884.1:n.-98C=
ENST00000551576.5:c.-5-135C= ENSP00000455848.1:n.-5-135C=
NM_000020.2:c.-5-135C= , LRG_543t1:c.-5-135C= NP_000011.2:n.-5-135C=
NM_001077401.1:c.-140C= NP_001070869.1:n.-140C=
XM_005269235.2:c.-5-135C= XP_005269292.1:n.-5-135C=
XM_011539008.1:c.-98C= XP_011537310.1:n.-98C=
NM_000020.3:c.-5-135C= MANE Select NP_000011.2:n.-5-135C=