Canonical Allele Identifier: CA2618861192
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920942_51920946dup , CM000674.2:g.51920942_51920946dup GRCh38
NC_000012.11:g.52314726_52314730dup , CM000674.1:g.52314726_52314730dup GRCh37
NC_000012.10:g.50600993_50600997dup NCBI36
NG_009549.1:g.18525_18529dup , LRG_543:g.18525_18529dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*49_*53dup ENSP00000455848.2:n.*49_*53dup
ENST00000388922.9:c.*49_*53dup MANE Select ENSP00000373574.4:n.*49_*53dup
ENST00000388922.8:c.*49_*53dup ENSP00000373574.4:n.*49_*53dup
ENST00000419526.6:c.*49_*53dup ENSP00000392492.2:n.*49_*53dup
ENST00000550683.5:c.*49_*53dup ENSP00000447884.1:n.*49_*53dup
NM_000020.2:c.*49_*53dup , LRG_543t1:c.*49_*53dup NP_000011.2:n.*49_*53dup
NM_001077401.1:c.*49_*53dup NP_001070869.1:n.*49_*53dup
XM_005269235.2:c.*49_*53dup XP_005269292.1:n.*49_*53dup
XM_011539008.1:c.*49_*53dup XP_011537310.1:n.*49_*53dup
XM_024449279.1:c.*49_*53dup XP_024305047.1:n.*49_*53dup
NM_000020.3:c.*49_*53dup MANE Select NP_000011.2:n.*49_*53dup
NM_001077401.2:c.*49_*53dup NP_001070869.1:n.*49_*53dup