Canonical Allele Identifier: CA2618858089

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51915511-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915515del , CM000674.2:g.51915515del	GRCh38
NC_000012.11:g.52309299del , CM000674.1:g.52309299del	GRCh37
NC_000012.10:g.50595566del	NCBI36
NG_009549.1:g.13098del , LRG_543:g.13098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.778+15del	ENSP00000446724.2:n.778+15del
ENST00000551576.6:c.1048+15del	ENSP00000455848.2:n.1048+15del
ENST00000552678.2:c.1048+15del	ENSP00000457394.2:n.1048+15del
ENST00000388922.9:c.1048+15del MANE Select	ENSP00000373574.4:n.1048+15del
ENST00000388922.8:c.1048+15del	ENSP00000373574.4:n.1048+15del
ENST00000419526.6:c.526+15del	ENSP00000392492.2:n.526+15del
ENST00000550683.5:c.1090+15del	ENSP00000447884.1:n.1090+15del
ENST00000552678.1:c.53+15del
NM_000020.2:c.1048+15del , LRG_543t1:c.1048+15del	NP_000011.2:n.1048+15del
NM_001077401.1:c.1048+15del	NP_001070869.1:n.1048+15del
XM_005269235.2:c.1048+15del	XP_005269292.1:n.1048+15del
XM_011539008.1:c.778+15del	XP_011537310.1:n.778+15del
XM_024449279.1:c.259+15del	XP_024305047.1:n.259+15del
NM_000020.3:c.1048+15del MANE Select	NP_000011.2:n.1048+15del
NM_001077401.2:c.1048+15del	NP_001070869.1:n.1048+15del