Canonical Allele Identifier: CA2618860413

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51920919-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920919_51920920insGGG , CM000674.2:g.51920919_51920920insGGG	GRCh38
NC_000012.11:g.52314703_52314704insGGG , CM000674.1:g.52314703_52314704insGGG	GRCh37
NC_000012.10:g.50600970_50600971insGGG	NCBI36
NG_009549.1:g.18502_18503insGGG , LRG_543:g.18502_18503insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*26_*27insGGG	ENSP00000455848.2:n.*26_*27insGGG
ENST00000388922.9:c.*26_*27insGGG MANE Select	ENSP00000373574.4:n.*26_*27insGGG
ENST00000388922.8:c.*26_*27insGGG	ENSP00000373574.4:n.*26_*27insGGG
ENST00000419526.6:c.*26_*27insGGG	ENSP00000392492.2:n.*26_*27insGGG
ENST00000550683.5:c.*26_*27insGGG	ENSP00000447884.1:n.*26_*27insGGG
NM_000020.2:c.*26_*27insGGG , LRG_543t1:c.*26_*27insGGG	NP_000011.2:n.*26_*27insGGG
NM_001077401.1:c.*26_*27insGGG	NP_001070869.1:n.*26_*27insGGG
XM_005269235.2:c.*26_*27insGGG	XP_005269292.1:n.*26_*27insGGG
XM_011539008.1:c.*26_*27insGGG	XP_011537310.1:n.*26_*27insGGG
XM_024449279.1:c.*26_*27insGGG	XP_024305047.1:n.*26_*27insGGG
NM_000020.3:c.*26_*27insGGG MANE Select	NP_000011.2:n.*26_*27insGGG
NM_001077401.2:c.*26_*27insGGG	NP_001070869.1:n.*26_*27insGGG