Canonical Allele Identifier: CA2795983941
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920941_51920942insTGGGGGGG , CM000674.2:g.51920941_51920942insTGGGGGGG GRCh38
NC_000012.11:g.52314725_52314726insTGGGGGGG , CM000674.1:g.52314725_52314726insTGGGGGGG GRCh37
NC_000012.10:g.50600992_50600993insTGGGGGGG NCBI36
NG_009549.1:g.18524_18525insTGGGGGGG , LRG_543:g.18524_18525insTGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*48_*49insTGGGGGGG ENSP00000455848.2:n.*48_*49insTGGGGGGG
ENST00000388922.9:c.*48_*49insTGGGGGGG MANE Select ENSP00000373574.4:n.*48_*49insTGGGGGGG
ENST00000388922.8:c.*48_*49insTGGGGGGG ENSP00000373574.4:n.*48_*49insTGGGGGGG
ENST00000419526.6:c.*48_*49insTGGGGGGG ENSP00000392492.2:n.*48_*49insTGGGGGGG
ENST00000550683.5:c.*48_*49insTGGGGGGG ENSP00000447884.1:n.*48_*49insTGGGGGGG
NM_000020.2:c.*48_*49insTGGGGGGG , LRG_543t1:c.*48_*49insTGGGGGGG NP_000011.2:n.*48_*49insTGGGGGGG
NM_001077401.1:c.*48_*49insTGGGGGGG NP_001070869.1:n.*48_*49insTGGGGGGG
XM_005269235.2:c.*48_*49insTGGGGGGG XP_005269292.1:n.*48_*49insTGGGGGGG
XM_011539008.1:c.*48_*49insTGGGGGGG XP_011537310.1:n.*48_*49insTGGGGGGG
XM_024449279.1:c.*48_*49insTGGGGGGG XP_024305047.1:n.*48_*49insTGGGGGGG
NM_000020.3:c.*48_*49insTGGGGGGG MANE Select NP_000011.2:n.*48_*49insTGGGGGGG
NM_001077401.2:c.*48_*49insTGGGGGGG NP_001070869.1:n.*48_*49insTGGGGGGG