Canonical Allele Identifier: CA2618860457

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51920930-C-CGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920930_51920931insGGGGGGGGGGGGGGGGGGG , CM000674.2:g.51920930_51920931insGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000012.11:g.52314714_52314715insGGGGGGGGGGGGGGGGGGG , CM000674.1:g.52314714_52314715insGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000012.10:g.50600981_50600982insGGGGGGGGGGGGGGGGGGG	NCBI36
NG_009549.1:g.18513_18514insGGGGGGGGGGGGGGGGGGG , LRG_543:g.18513_18514insGGGGGGGGGGGGGGGGGGG

Transcript Alleles

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