Canonical Allele Identifier: CA2618860828

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51920934-GGGGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920939_51920943del , CM000674.2:g.51920939_51920943del	GRCh38
NC_000012.11:g.52314723_52314727del , CM000674.1:g.52314723_52314727del	GRCh37
NC_000012.10:g.50600990_50600994del	NCBI36
NG_009549.1:g.18522_18526del , LRG_543:g.18522_18526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*46_*50del	ENSP00000455848.2:n.*46_*50del
ENST00000388922.9:c.*46_*50del MANE Select	ENSP00000373574.4:n.*46_*50del
ENST00000388922.8:c.*46_*50del	ENSP00000373574.4:n.*46_*50del
ENST00000419526.6:c.*46_*50del	ENSP00000392492.2:n.*46_*50del
ENST00000550683.5:c.*46_*50del	ENSP00000447884.1:n.*46_*50del
NM_000020.2:c.*46_*50del , LRG_543t1:c.*46_*50del	NP_000011.2:n.*46_*50del
NM_001077401.1:c.*46_*50del	NP_001070869.1:n.*46_*50del
XM_005269235.2:c.*46_*50del	XP_005269292.1:n.*46_*50del
XM_011539008.1:c.*46_*50del	XP_011537310.1:n.*46_*50del
XM_024449279.1:c.*46_*50del	XP_024305047.1:n.*46_*50del
NM_000020.3:c.*46_*50del MANE Select	NP_000011.2:n.*46_*50del
NM_001077401.2:c.*46_*50del	NP_001070869.1:n.*46_*50del