Canonical Allele Identifier: CA2036267366
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913338_51913339delinsCT , CM000674.2:g.51913338_51913339delinsCT GRCh38
NC_000012.11:g.52307122_52307123delinsCT , CM000674.1:g.52307122_52307123delinsCT GRCh37
NC_000012.10:g.50593389_50593390delinsCT NCBI36
NG_009549.1:g.10921_10922delinsCT , LRG_543:g.10921_10922delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.343_344delinsCT ENSP00000446724.2:p.Leu115=
ENST00000551576.6:c.301_302delinsCT ENSP00000455848.2:p.Leu101=
ENST00000552678.2:c.301_302delinsCT ENSP00000457394.2:p.Leu101=
ENST00000388922.9:c.301_302delinsCT MANE Select ENSP00000373574.4:p.Leu101=
ENST00000388922.8:c.301_302delinsCT ENSP00000373574.4:p.Leu101=
ENST00000419526.6:c.103+803_103+804delinsCT ENSP00000392492.2:n.103+803_103+804delins...
ENST00000547400.5:c.343_344delinsCT ENSP00000446724.1:p.Leu115=
ENST00000550683.5:c.343_344delinsCT ENSP00000447884.1:p.Leu115=
NM_000020.2:c.301_302delinsCT , LRG_543t1:c.301_302delinsCT NP_000011.2:p.Leu101=
NM_001077401.1:c.301_302delinsCT NP_001070869.1:p.Leu101=
XM_005269235.2:c.301_302delinsCT XP_005269292.1:p.Leu101=
XM_011539008.1:c.343_344delinsCT XP_011537310.1:p.Leu115=
XM_024449279.1:c.-389_-388delinsCT XP_024305047.1:n.-389_-388delinsCT
NM_000020.3:c.301_302delinsCT MANE Select NP_000011.2:p.Leu101=
NM_001077401.2:c.301_302delinsCT NP_001070869.1:p.Leu101=