Canonical Allele Identifier: CA2618857212

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51915168-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915170del , CM000674.2:g.51915170del	GRCh38
NC_000012.11:g.52308954del , CM000674.1:g.52308954del	GRCh37
NC_000012.10:g.50595221del	NCBI36
NG_009549.1:g.12753del , LRG_543:g.12753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.503-55del	ENSP00000446724.2:n.503-55del
ENST00000551576.6:c.773-55del	ENSP00000455848.2:n.773-55del
ENST00000552678.2:c.773-55del	ENSP00000457394.2:n.773-55del
ENST00000388922.9:c.773-55del MANE Select	ENSP00000373574.4:n.773-55del
ENST00000388922.8:c.773-55del	ENSP00000373574.4:n.773-55del
ENST00000419526.6:c.251-55del	ENSP00000392492.2:n.251-55del
ENST00000550683.5:c.815-55del	ENSP00000447884.1:n.815-55del
NM_000020.2:c.773-55del , LRG_543t1:c.773-55del	NP_000011.2:n.773-55del
NM_001077401.1:c.773-55del	NP_001070869.1:n.773-55del
XM_005269235.2:c.773-55del	XP_005269292.1:n.773-55del
XM_011539008.1:c.503-55del	XP_011537310.1:n.503-55del
XM_024449279.1:c.-17-55del	XP_024305047.1:n.-17-55del
NM_000020.3:c.773-55del MANE Select	NP_000011.2:n.773-55del
NM_001077401.2:c.773-55del	NP_001070869.1:n.773-55del