Canonical Allele Identifier: CA2036242326

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51921156_51921157delinsCT , CM000674.2:g.51921156_51921157delinsCT	GRCh38
NC_000012.11:g.52314940_52314941delinsCT , CM000674.1:g.52314940_52314941delinsCT	GRCh37
NC_000012.10:g.50601207_50601208delinsCT	NCBI36
NG_009549.1:g.18739_18740delinsCT , LRG_543:g.18739_18740delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*263_*264delinsCT	ENSP00000455848.2:n.*263_*264delinsCT
ENST00000388922.9:c.*263_*264delinsCT MANE Select	ENSP00000373574.4:n.*263_*264delinsCT
ENST00000419526.6:c.*263_*264delinsCT	ENSP00000392492.2:n.*263_*264delinsCT
ENST00000550683.5:c.*263_*264delinsCT	ENSP00000447884.1:n.*263_*264delinsCT
NM_000020.2:c.*263_*264delinsCT , LRG_543t1:c.*263_*264delinsCT	NP_000011.2:n.*263_*264delinsCT
NM_001077401.1:c.*263_*264delinsCT	NP_001070869.1:n.*263_*264delinsCT
XM_005269235.2:c.*263_*264delinsCT	XP_005269292.1:n.*263_*264delinsCT
XM_011539008.1:c.*263_*264delinsCT	XP_011537310.1:n.*263_*264delinsCT
XM_024449279.1:c.*263_*264delinsCT	XP_024305047.1:n.*263_*264delinsCT
NM_000020.3:c.*263_*264delinsCT MANE Select	NP_000011.2:n.*263_*264delinsCT
NM_001077401.2:c.*263_*264delinsCT	NP_001070869.1:n.*263_*264delinsCT