Canonical Allele Identifier: CA919069745
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs1592407671

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429242_40429243insGGG , CM000674.2:g.40429242_40429243insGGG GRCh38
NC_000012.11:g.40823044_40823045insGGG , CM000674.1:g.40823044_40823045insGGG GRCh37
NC_000012.10:g.39109311_39109312insGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2397-300_2397-299insGGG ENSP00000508949.1:n.2397-300_2397-299insGGG
ENST00000454784.9:n.2443-300_2443-299insGGG
NM_173600.2:c.2397-300_2397-299insGGG NP_775871.2:n.2397-300_2397-299insGGG
XR_944866.1:n.75-8930_75-8929insCCC
XR_944867.1:n.75-8930_75-8929insCCC
XR_944868.1:n.75-8930_75-8929insCCC
XR_944869.1:n.75-8930_75-8929insCCC
XR_944870.1:n.75-8930_75-8929insCCC
XR_944871.1:n.75-8930_75-8929insCCC
XR_944872.1:n.81-8930_81-8929insCCC
XR_944873.1:n.75-8930_75-8929insCCC
XR_001749087.1:n.75-8930_75-8929insCCC
XR_001749088.1:n.75-8930_75-8929insCCC
XR_944868.2:n.75-8930_75-8929insCCC
XR_944869.2:n.75-8930_75-8929insCCC