Canonical Allele Identifier: CA2618861005
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920940_51920941insTGGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.51920940_51920941insTGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.52314724_52314725insTGGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.52314724_52314725insTGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.50600991_50600992insTGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_009549.1:g.18523_18524insTGGGGGGGGGGGGGGGGGGGGGG , LRG_543:g.18523_18524insTGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG ENSP00000455848.2:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.9:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000373574.4:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.8:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG ENSP00000373574.4:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
ENST00000419526.6:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG ENSP00000392492.2:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
ENST00000550683.5:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG ENSP00000447884.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
NM_000020.2:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG , LRG_543t1:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG NP_000011.2:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.1:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
XM_005269235.2:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG XP_005269292.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
XM_011539008.1:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG XP_011537310.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
XM_024449279.1:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG XP_024305047.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
NM_000020.3:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000011.2:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.2:c.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*47_*48insTGGGGGGGGGGGGGGGGGGGGGG