Canonical Allele Identifier: CA2575161703
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920944_51920945insAG , CM000674.2:g.51920944_51920945insAG GRCh38
NC_000012.11:g.52314728_52314729insAG , CM000674.1:g.52314728_52314729insAG GRCh37
NC_000012.10:g.50600995_50600996insAG NCBI36
NG_009549.1:g.18527_18528insAG , LRG_543:g.18527_18528insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*51_*52insAG ENSP00000455848.2:n.*51_*52insAG
ENST00000388922.9:c.*51_*52insAG MANE Select ENSP00000373574.4:n.*51_*52insAG
ENST00000388922.8:c.*51_*52insAG ENSP00000373574.4:n.*51_*52insAG
ENST00000419526.6:c.*51_*52insAG ENSP00000392492.2:n.*51_*52insAG
ENST00000550683.5:c.*51_*52insAG ENSP00000447884.1:n.*51_*52insAG
NM_000020.2:c.*51_*52insAG , LRG_543t1:c.*51_*52insAG NP_000011.2:n.*51_*52insAG
NM_001077401.1:c.*51_*52insAG NP_001070869.1:n.*51_*52insAG
XM_005269235.2:c.*51_*52insAG XP_005269292.1:n.*51_*52insAG
XM_011539008.1:c.*51_*52insAG XP_011537310.1:n.*51_*52insAG
XM_024449279.1:c.*51_*52insAG XP_024305047.1:n.*51_*52insAG
NM_000020.3:c.*51_*52insAG MANE Select NP_000011.2:n.*51_*52insAG
NM_001077401.2:c.*51_*52insAG NP_001070869.1:n.*51_*52insAG