Canonical Allele Identifier: CA2618860750
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920938_51920939insGGGGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.51920938_51920939insGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.52314722_52314723insGGGGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.52314722_52314723insGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.50600989_50600990insGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_009549.1:g.18521_18522insGGGGGGGGGGGGGGGGGGGGGGGG , LRG_543:g.18521_18522insGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000455848.2:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.9:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000373574.4:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000388922.8:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000373574.4:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000419526.6:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000392492.2:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000550683.5:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000447884.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
NM_000020.2:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG , LRG_543t1:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG NP_000011.2:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.1:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
XM_005269235.2:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG XP_005269292.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
XM_011539008.1:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG XP_011537310.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
XM_024449279.1:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG XP_024305047.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
NM_000020.3:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000011.2:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG
NM_001077401.2:c.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG NP_001070869.1:n.*45_*46insGGGGGGGGGGGGGGGGGGGGGGGG