Canonical Allele Identifier: CA2618860852

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51920937-GGTGGGGGGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920942_51920951del , CM000674.2:g.51920942_51920951del	GRCh38
NC_000012.11:g.52314726_52314735del , CM000674.1:g.52314726_52314735del	GRCh37
NC_000012.10:g.50600993_50601002del	NCBI36
NG_009549.1:g.18525_18534del , LRG_543:g.18525_18534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*49_*58del	ENSP00000455848.2:n.*49_*58del
ENST00000388922.9:c.*49_*58del MANE Select	ENSP00000373574.4:n.*49_*58del
ENST00000388922.8:c.*49_*58del	ENSP00000373574.4:n.*49_*58del
ENST00000419526.6:c.*49_*58del	ENSP00000392492.2:n.*49_*58del
ENST00000550683.5:c.*49_*58del	ENSP00000447884.1:n.*49_*58del
NM_000020.2:c.*49_*58del , LRG_543t1:c.*49_*58del	NP_000011.2:n.*49_*58del
NM_001077401.1:c.*49_*58del	NP_001070869.1:n.*49_*58del
XM_005269235.2:c.*49_*58del	XP_005269292.1:n.*49_*58del
XM_011539008.1:c.*49_*58del	XP_011537310.1:n.*49_*58del
XM_024449279.1:c.*49_*58del	XP_024305047.1:n.*49_*58del
NM_000020.3:c.*49_*58del MANE Select	NP_000011.2:n.*49_*58del
NM_001077401.2:c.*49_*58del	NP_001070869.1:n.*49_*58del