Canonical Allele Identifier: CA2036267582

Gene: ACVRL1

Linked Data

• dbSNP Id: rs1940745062
• gnomAD v4: 12-51913444-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913449del , CM000674.2:g.51913449del	GRCh38
NC_000012.11:g.52307233del , CM000674.1:g.52307233del	GRCh37
NC_000012.10:g.50593500del	NCBI36
NG_009549.1:g.11032del , LRG_543:g.11032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+99del	ENSP00000446724.2:n.355+99del
ENST00000551576.6:c.313+99del	ENSP00000455848.2:n.313+99del
ENST00000552678.2:c.313+99del	ENSP00000457394.2:n.313+99del
ENST00000388922.9:c.313+99del MANE Select	ENSP00000373574.4:n.313+99del
ENST00000388922.8:c.313+99del	ENSP00000373574.4:n.313+99del
ENST00000419526.6:c.103+914del	ENSP00000392492.2:n.103+914del
ENST00000547400.5:c.355+99del	ENSP00000446724.1:n.355+99del
ENST00000550683.5:c.355+99del	ENSP00000447884.1:n.355+99del
NM_000020.2:c.313+99del , LRG_543t1:c.313+99del	NP_000011.2:n.313+99del
NM_001077401.1:c.313+99del	NP_001070869.1:n.313+99del
XM_005269235.2:c.313+99del	XP_005269292.1:n.313+99del
XM_011539008.1:c.355+99del	XP_011537310.1:n.355+99del
XM_024449279.1:c.-377+99del	XP_024305047.1:n.-377+99del
NM_000020.3:c.313+99del MANE Select	NP_000011.2:n.313+99del
NM_001077401.2:c.313+99del	NP_001070869.1:n.313+99del