Canonical Allele Identifier: CA2575161634

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920723_51920724del , CM000674.2:g.51920723_51920724del	GRCh38
NC_000012.11:g.52314507_52314508del , CM000674.1:g.52314507_52314508del	GRCh37
NC_000012.10:g.50600774_50600775del	NCBI36
NG_009549.1:g.18306_18307del , LRG_543:g.18306_18307del

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.1108-36_1108-35del	ENSP00000446724.2:n.1108-36_1108-35del
ENST00000551576.6:c.1378-36_1378-35del	ENSP00000455848.2:n.1378-36_1378-35del
ENST00000388922.9:c.1378-36_1378-35del MANE Select	ENSP00000373574.4:n.1378-36_1378-35del
ENST00000388922.8:c.1378-36_1378-35del	ENSP00000373574.4:n.1378-36_1378-35del
ENST00000419526.6:c.856-36_856-35del	ENSP00000392492.2:n.856-36_856-35del
ENST00000550683.5:c.1420-36_1420-35del	ENSP00000447884.1:n.1420-36_1420-35del
NM_000020.2:c.1378-36_1378-35del , LRG_543t1:c.1378-36_1378-35del	NP_000011.2:n.1378-36_1378-35del
NM_001077401.1:c.1378-36_1378-35del	NP_001070869.1:n.1378-36_1378-35del
XM_005269235.2:c.1378-36_1378-35del	XP_005269292.1:n.1378-36_1378-35del
XM_011539008.1:c.1108-36_1108-35del	XP_011537310.1:n.1108-36_1108-35del
XM_024449279.1:c.589-36_589-35del	XP_024305047.1:n.589-36_589-35del
NM_000020.3:c.1378-36_1378-35del MANE Select	NP_000011.2:n.1378-36_1378-35del
NM_001077401.2:c.1378-36_1378-35del	NP_001070869.1:n.1378-36_1378-35del