Canonical Allele Identifier: CA2618860961
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920943_51920944insTGGGGGGGGGGGGGGG , CM000674.2:g.51920943_51920944insTGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.52314727_52314728insTGGGGGGGGGGGGGGG , CM000674.1:g.52314727_52314728insTGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.50600994_50600995insTGGGGGGGGGGGGGGG NCBI36
NG_009549.1:g.18526_18527insTGGGGGGGGGGGGGGG , LRG_543:g.18526_18527insTGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*50_*51insTGGGGGGGGGGGGGGG ENSP00000455848.2:n.*50_*51insTGGGGGGGGGGGGGGG
ENST00000388922.9:c.*50_*51insTGGGGGGGGGGGGGGG MANE Select ENSP00000373574.4:n.*50_*51insTGGGGGGGGGGGGGGG
ENST00000388922.8:c.*50_*51insTGGGGGGGGGGGGGGG ENSP00000373574.4:n.*50_*51insTGGGGGGGGGGGGGGG
ENST00000419526.6:c.*50_*51insTGGGGGGGGGGGGGGG ENSP00000392492.2:n.*50_*51insTGGGGGGGGGGGGGGG
ENST00000550683.5:c.*50_*51insTGGGGGGGGGGGGGGG ENSP00000447884.1:n.*50_*51insTGGGGGGGGGGGGGGG
NM_000020.2:c.*50_*51insTGGGGGGGGGGGGGGG , LRG_543t1:c.*50_*51insTGGGGGGGGGGGGGGG NP_000011.2:n.*50_*51insTGGGGGGGGGGGGGGG
NM_001077401.1:c.*50_*51insTGGGGGGGGGGGGGGG NP_001070869.1:n.*50_*51insTGGGGGGGGGGGGGGG
XM_005269235.2:c.*50_*51insTGGGGGGGGGGGGGGG XP_005269292.1:n.*50_*51insTGGGGGGGGGGGGGGG
XM_011539008.1:c.*50_*51insTGGGGGGGGGGGGGGG XP_011537310.1:n.*50_*51insTGGGGGGGGGGGGGGG
XM_024449279.1:c.*50_*51insTGGGGGGGGGGGGGGG XP_024305047.1:n.*50_*51insTGGGGGGGGGGGGGGG
NM_000020.3:c.*50_*51insTGGGGGGGGGGGGGGG MANE Select NP_000011.2:n.*50_*51insTGGGGGGGGGGGGGGG
NM_001077401.2:c.*50_*51insTGGGGGGGGGGGGGGG NP_001070869.1:n.*50_*51insTGGGGGGGGGGGGGGG