Canonical Allele Identifier: CA2695216659

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51912524_51912527del , CM000674.2:g.51912524_51912527del	GRCh38
NC_000012.11:g.52306308_52306311del , CM000674.1:g.52306308_52306311del	GRCh37
NC_000012.10:g.50592575_50592578del	NCBI36
NG_009549.1:g.10107_10110del , LRG_543:g.10107_10110del

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.92_95del	ENSP00000446724.2:p.Leu31Ter
ENST00000551576.6:c.50_53del	ENSP00000455848.2:p.Leu17Ter
ENST00000552678.2:c.50_53del	ENSP00000457394.2:p.Leu17Ter
ENST00000388922.9:c.50_53del MANE Select	ENSP00000373574.4:p.Leu17Ter
ENST00000388922.8:c.50_53del	ENSP00000373574.4:p.Leu17Ter
ENST00000419526.6:c.92_95del	ENSP00000392492.2:p.Leu31Ter
ENST00000547400.5:c.92_95del	ENSP00000446724.1:p.Leu31Ter
ENST00000550683.5:c.92_95del	ENSP00000447884.1:p.Leu31Ter
ENST00000551576.5:c.50_53del	ENSP00000455848.1:p.Leu17Ter
NM_000020.2:c.50_53del , LRG_543t1:c.50_53del	NP_000011.2:p.Leu17Ter
NM_001077401.1:c.50_53del	NP_001070869.1:p.Leu17Ter
XM_005269235.2:c.50_53del	XP_005269292.1:p.Leu17Ter
XM_011539008.1:c.92_95del	XP_011537310.1:p.Leu31Ter
NM_000020.3:c.50_53del MANE Select	NP_000011.2:p.Leu17Ter
NM_001077401.2:c.50_53del	NP_001070869.1:p.Leu17Ter