Canonical Allele Identifier: CA2618860670
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920937_51920938insTTGGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.51920937_51920938insTTGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.52314721_52314722insTTGGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.52314721_52314722insTTGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.50600988_50600989insTTGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_009549.1:g.18520_18521insTTGGGGGGGGGGGGGGGGGGGGGG , LRG_543:g.18520_18521insTTGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG ENSP00000455848.2:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.9:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000373574.4:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.8:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG ENSP00000373574.4:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
ENST00000419526.6:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG ENSP00000392492.2:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
ENST00000550683.5:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG ENSP00000447884.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
NM_000020.2:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG , LRG_543t1:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG NP_000011.2:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.1:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
XM_005269235.2:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG XP_005269292.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
XM_011539008.1:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG XP_011537310.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
XM_024449279.1:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG XP_024305047.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
NM_000020.3:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000011.2:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.2:c.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*44_*45insTTGGGGGGGGGGGGGGGGGGGGGG