Canonical Allele Identifier: CA2036241918
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920836_51920839delinsCAAG , CM000674.2:g.51920836_51920839delinsCAAG GRCh38
NC_000012.11:g.52314620_52314623delinsCAAG , CM000674.1:g.52314620_52314623delinsCAAG GRCh37
NC_000012.10:g.50600887_50600890delinsCAAG NCBI36
NG_009549.1:g.18419_18422delinsCAAG , LRG_543:g.18419_18422delinsCAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000388922.9:c.1455_1458delinsCAAG MANE Select ENSP00000373574.4:p.Ile485=
ENST00000388922.8:c.1455_1458delinsCAAG ENSP00000373574.4:p.Ile485=
ENST00000419526.6:c.933_936delinsCAAG ENSP00000392492.2:p.Ile311=
ENST00000550683.5:c.1497_1500delinsCAAG ENSP00000447884.1:p.Ile499=
NM_000020.2:c.1455_1458delinsCAAG , LRG_543t1:c.1455_1458delinsCAAG NP_000011.2:p.Ile485=
NM_001077401.1:c.1455_1458delinsCAAG NP_001070869.1:p.Ile485=
XM_005269235.2:c.1455_1458delinsCAAG XP_005269292.1:p.Ile485=
XM_011539008.1:c.1185_1188delinsCAAG XP_011537310.1:p.Ile395=
XM_024449279.1:c.666_669delinsCAAG XP_024305047.1:p.Ile222=
NM_000020.3:c.1455_1458delinsCAAG MANE Select NP_000011.2:p.Ile485=
NM_001077401.2:c.1455_1458delinsCAAG NP_001070869.1:p.Ile485=