Canonical Allele Identifier: CA2839074598
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913082dup , CM000674.2:g.51913082dup GRCh38
NC_000012.11:g.52306866dup , CM000674.1:g.52306866dup GRCh37
NC_000012.10:g.50593133dup NCBI36
NG_009549.1:g.10665dup , LRG_543:g.10665dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.104-17dup ENSP00000446724.2:n.104-17dup
ENST00000551576.6:c.62-17dup ENSP00000455848.2:n.62-17dup
ENST00000552678.2:c.62-17dup ENSP00000457394.2:n.62-17dup
ENST00000388922.9:c.62-17dup MANE Select ENSP00000373574.4:n.62-17dup
ENST00000388922.8:c.62-17dup ENSP00000373574.4:n.62-17dup
ENST00000419526.6:c.103+547dup ENSP00000392492.2:n.103+547dup
ENST00000547400.5:c.104-17dup ENSP00000446724.1:n.104-17dup
ENST00000550683.5:c.104-17dup ENSP00000447884.1:n.104-17dup
ENST00000551576.5:c.62-17dup ENSP00000455848.1:n.62-17dup
NM_000020.2:c.62-17dup , LRG_543t1:c.62-17dup NP_000011.2:n.62-17dup
NM_001077401.1:c.62-17dup NP_001070869.1:n.62-17dup
XM_005269235.2:c.62-17dup XP_005269292.1:n.62-17dup
XM_011539008.1:c.104-17dup XP_011537310.1:n.104-17dup
NM_000020.3:c.62-17dup MANE Select NP_000011.2:n.62-17dup
NM_001077401.2:c.62-17dup NP_001070869.1:n.62-17dup