Canonical Allele Identifier: CA2618860447
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920930_51920931insAGGGGGG , CM000674.2:g.51920930_51920931insAGGGGGG GRCh38
NC_000012.11:g.52314714_52314715insAGGGGGG , CM000674.1:g.52314714_52314715insAGGGGGG GRCh37
NC_000012.10:g.50600981_50600982insAGGGGGG NCBI36
NG_009549.1:g.18513_18514insAGGGGGG , LRG_543:g.18513_18514insAGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*37_*38insAGGGGGG ENSP00000455848.2:n.*37_*38insAGGGGGG
ENST00000388922.9:c.*37_*38insAGGGGGG MANE Select ENSP00000373574.4:n.*37_*38insAGGGGGG
ENST00000388922.8:c.*37_*38insAGGGGGG ENSP00000373574.4:n.*37_*38insAGGGGGG
ENST00000419526.6:c.*37_*38insAGGGGGG ENSP00000392492.2:n.*37_*38insAGGGGGG
ENST00000550683.5:c.*37_*38insAGGGGGG ENSP00000447884.1:n.*37_*38insAGGGGGG
NM_000020.2:c.*37_*38insAGGGGGG , LRG_543t1:c.*37_*38insAGGGGGG NP_000011.2:n.*37_*38insAGGGGGG
NM_001077401.1:c.*37_*38insAGGGGGG NP_001070869.1:n.*37_*38insAGGGGGG
XM_005269235.2:c.*37_*38insAGGGGGG XP_005269292.1:n.*37_*38insAGGGGGG
XM_011539008.1:c.*37_*38insAGGGGGG XP_011537310.1:n.*37_*38insAGGGGGG
XM_024449279.1:c.*37_*38insAGGGGGG XP_024305047.1:n.*37_*38insAGGGGGG
NM_000020.3:c.*37_*38insAGGGGGG MANE Select NP_000011.2:n.*37_*38insAGGGGGG
NM_001077401.2:c.*37_*38insAGGGGGG NP_001070869.1:n.*37_*38insAGGGGGG