Canonical Allele Identifier: CA2618861184
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920945_51920946insGGGGGGGGGGGGGGGGGGGCGGGG , CM000674.2:g.51920945_51920946insGGGGGGGGGGGGGGGGGGGCGGGG GRCh38
NC_000012.11:g.52314729_52314730insGGGGGGGGGGGGGGGGGGGCGGGG , CM000674.1:g.52314729_52314730insGGGGGGGGGGGGGGGGGGGCGGGG GRCh37
NC_000012.10:g.50600996_50600997insGGGGGGGGGGGGGGGGGGGCGGGG NCBI36
NG_009549.1:g.18528_18529insGGGGGGGGGGGGGGGGGGGCGGGG , LRG_543:g.18528_18529insGGGGGGGGGGGGGGGGGGGCGGGG

Transcript Alleles

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