Canonical Allele Identifier: CA688754677
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs1358276167

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429536dup , CM000674.2:g.40429536dup GRCh38
NC_000012.11:g.40823338dup , CM000674.1:g.40823338dup GRCh37
NC_000012.10:g.39109605dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2397-6dup ENSP00000508949.1:n.2397-6dup
ENST00000454784.9:n.2443-6dup
NM_173600.2:c.2397-6dup NP_775871.2:n.2397-6dup
XR_944866.1:n.75-9222dup
XR_944867.1:n.75-9222dup
XR_944868.1:n.75-9222dup
XR_944869.1:n.75-9222dup
XR_944870.1:n.75-9222dup
XR_944871.1:n.75-9222dup
XR_944872.1:n.81-9222dup
XR_944873.1:n.75-9222dup
XR_001749087.1:n.75-9222dup
XR_001749088.1:n.75-9222dup
XR_944868.2:n.75-9222dup
XR_944869.2:n.75-9222dup