Canonical Allele Identifier: CA605053106
Gene: ACVRL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52314709del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920929del , CM000674.2:g.51920929del GRCh38
NC_000012.11:g.52314713del , CM000674.1:g.52314713del GRCh37
NC_000012.10:g.50600980del NCBI36
NG_009549.1:g.18512del , LRG_543:g.18512del

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*36del ENSP00000455848.2:n.*36del
ENST00000388922.9:c.*36del MANE Select ENSP00000373574.4:n.*36del
ENST00000388922.8:c.*36del ENSP00000373574.4:n.*36del
ENST00000419526.6:c.*36del ENSP00000392492.2:n.*36del
ENST00000550683.5:c.*36del ENSP00000447884.1:n.*36del
NM_000020.2:c.*36del , LRG_543t1:c.*36del NP_000011.2:n.*36del
NM_001077401.1:c.*36del NP_001070869.1:n.*36del
XM_005269235.2:c.*36del XP_005269292.1:n.*36del
XM_011539008.1:c.*36del XP_011537310.1:n.*36del
XM_024449279.1:c.*36del XP_024305047.1:n.*36del
NM_000020.3:c.*36del MANE Select NP_000011.2:n.*36del
NM_001077401.2:c.*36del NP_001070869.1:n.*36del