Canonical Allele Identifier: CA2618860951
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920944_51920945insTGTGGGGGGGGGGGGG , CM000674.2:g.51920944_51920945insTGTGGGGGGGGGGGGG GRCh38
NC_000012.11:g.52314728_52314729insTGTGGGGGGGGGGGGG , CM000674.1:g.52314728_52314729insTGTGGGGGGGGGGGGG GRCh37
NC_000012.10:g.50600995_50600996insTGTGGGGGGGGGGGGG NCBI36
NG_009549.1:g.18527_18528insTGTGGGGGGGGGGGGG , LRG_543:g.18527_18528insTGTGGGGGGGGGGGGG

Transcript Alleles

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