Canonical Allele Identifier: CA604521819
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs1180058639
gnomAD v2: 12-40823065-AC-A
gnomAD v3: 12-40429263-AC-A
gnomAD v4: 12-40429263-AC-A
MyVariant Identifiers: chr12:g.40823066del (hg19) chr12:g.40429264del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429265del , CM000674.2:g.40429265del GRCh38
NC_000012.11:g.40823067del , CM000674.1:g.40823067del GRCh37
NC_000012.10:g.39109334del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2397-277del ENSP00000508949.1:n.2397-277del
ENST00000454784.9:n.2443-277del
NM_173600.2:c.2397-277del NP_775871.2:n.2397-277del
XR_944866.1:n.75-8953del
XR_944867.1:n.75-8953del
XR_944868.1:n.75-8953del
XR_944869.1:n.75-8953del
XR_944870.1:n.75-8953del
XR_944871.1:n.75-8953del
XR_944872.1:n.81-8953del
XR_944873.1:n.75-8953del
XR_001749087.1:n.75-8953del
XR_001749088.1:n.75-8953del
XR_944868.2:n.75-8953del
XR_944869.2:n.75-8953del
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