Canonical Allele Identifier: CA2618861361
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920945_51920946insGGGGGGGGGGGGGGGGGGGGCGGG , CM000674.2:g.51920945_51920946insGGGGGGGGGGGGGGGGGGGGCGGG GRCh38
NC_000012.11:g.52314729_52314730insGGGGGGGGGGGGGGGGGGGGCGGG , CM000674.1:g.52314729_52314730insGGGGGGGGGGGGGGGGGGGGCGGG GRCh37
NC_000012.10:g.50600996_50600997insGGGGGGGGGGGGGGGGGGGGCGGG NCBI36
NG_009549.1:g.18528_18529insGGGGGGGGGGGGGGGGGGGGCGGG , LRG_543:g.18528_18529insGGGGGGGGGGGGGGGGGGGGCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG ENSP00000455848.2:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
ENST00000388922.9:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG MANE Select ENSP00000373574.4:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
ENST00000388922.8:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG ENSP00000373574.4:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
ENST00000419526.6:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG ENSP00000392492.2:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
ENST00000550683.5:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG ENSP00000447884.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
NM_000020.2:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG , LRG_543t1:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG NP_000011.2:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
NM_001077401.1:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG NP_001070869.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
XM_005269235.2:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG XP_005269292.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
XM_011539008.1:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG XP_011537310.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
XM_024449279.1:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG XP_024305047.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
NM_000020.3:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG MANE Select NP_000011.2:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG
NM_001077401.2:c.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG NP_001070869.1:n.*52_*53insGGGGGGGGGGGGGGGGGGGGCGGG