Canonical Allele Identifier: CA2977854252
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920735dup , CM000674.2:g.51920735dup GRCh38
NC_000012.11:g.52314519dup , CM000674.1:g.52314519dup GRCh37
NC_000012.10:g.50600786dup NCBI36
NG_009549.1:g.18318dup , LRG_543:g.18318dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.1108-24dup ENSP00000446724.2:n.1108-24dup
ENST00000551576.6:c.1378-24dup ENSP00000455848.2:n.1378-24dup
ENST00000388922.9:c.1378-24dup MANE Select ENSP00000373574.4:n.1378-24dup
ENST00000388922.8:c.1378-24dup ENSP00000373574.4:n.1378-24dup
ENST00000419526.6:c.856-24dup ENSP00000392492.2:n.856-24dup
ENST00000550683.5:c.1420-24dup ENSP00000447884.1:n.1420-24dup
NM_000020.2:c.1378-24dup , LRG_543t1:c.1378-24dup NP_000011.2:n.1378-24dup
NM_001077401.1:c.1378-24dup NP_001070869.1:n.1378-24dup
XM_005269235.2:c.1378-24dup XP_005269292.1:n.1378-24dup
XM_011539008.1:c.1108-24dup XP_011537310.1:n.1108-24dup
XM_024449279.1:c.589-24dup XP_024305047.1:n.589-24dup
NM_000020.3:c.1378-24dup MANE Select NP_000011.2:n.1378-24dup
NM_001077401.2:c.1378-24dup NP_001070869.1:n.1378-24dup