Canonical Allele Identifier: CA2618860718

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51920931-T-TGGGGGTGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920936_51920937insTGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.51920936_51920937insTGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000012.11:g.52314720_52314721insTGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.52314720_52314721insTGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000012.10:g.50600987_50600988insTGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_009549.1:g.18519_18520insTGGGGGGGGGGGGGGGGGGGGG , LRG_543:g.18519_18520insTGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	ENSP00000455848.2:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.9:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000373574.4:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.8:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	ENSP00000373574.4:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
ENST00000419526.6:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	ENSP00000392492.2:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
ENST00000550683.5:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	ENSP00000447884.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
NM_000020.2:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG , LRG_543t1:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	NP_000011.2:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
NM_001077401.1:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	NP_001070869.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
XM_005269235.2:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	XP_005269292.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
XM_011539008.1:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	XP_011537310.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
XM_024449279.1:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	XP_024305047.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
NM_000020.3:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_000011.2:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG
NM_001077401.2:c.*43_*44insTGGGGGGGGGGGGGGGGGGGGG	NP_001070869.1:n.*43_*44insTGGGGGGGGGGGGGGGGGGGGG