Canonical Allele Identifier: CA2695216670

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913192del , CM000674.2:g.51913192del	GRCh38
NC_000012.11:g.52306976del , CM000674.1:g.52306976del	GRCh37
NC_000012.10:g.50593243del	NCBI36
NG_009549.1:g.10775del , LRG_543:g.10775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.197del	ENSP00000446724.2:p.Thr66LysfsTer2
ENST00000551576.6:c.155del	ENSP00000455848.2:p.Thr52LysfsTer2
ENST00000552678.2:c.155del	ENSP00000457394.2:p.Thr52LysfsTer2
ENST00000388922.9:c.155del MANE Select	ENSP00000373574.4:p.Thr52LysfsTer2
ENST00000388922.8:c.155del	ENSP00000373574.4:p.Thr52LysfsTer2
ENST00000419526.6:c.103+657del	ENSP00000392492.2:n.103+657del
ENST00000547400.5:c.197del	ENSP00000446724.1:p.Thr66LysfsTer2
ENST00000550683.5:c.197del	ENSP00000447884.1:p.Thr66LysfsTer2
ENST00000551576.5:c.155del	ENSP00000455848.1:p.Thr52LysfsTer2
NM_000020.2:c.155del , LRG_543t1:c.155del	NP_000011.2:p.Thr52LysfsTer2
NM_001077401.1:c.155del	NP_001070869.1:p.Thr52LysfsTer2
XM_005269235.2:c.155del	XP_005269292.1:p.Thr52LysfsTer2
XM_011539008.1:c.197del	XP_011537310.1:p.Thr66LysfsTer2
NM_000020.3:c.155del MANE Select	NP_000011.2:p.Thr52LysfsTer2
NM_001077401.2:c.155del	NP_001070869.1:p.Thr52LysfsTer2