Canonical Allele Identifier: CA688754392

Gene: MUC19

Linked Data

• dbSNP Id: rs1166042742
• MyVariant Identifiers: chr12:g.40822917_40822918del (hg19) ; chr12:g.40429115_40429116del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40429115_40429116del , CM000674.2:g.40429115_40429116del	GRCh38
NC_000012.11:g.40822917_40822918del , CM000674.1:g.40822917_40822918del	GRCh37
NC_000012.10:g.39109184_39109185del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454784.10:c.2397-427_2397-426del	ENSP00000508949.1:n.2397-427_2397-426del
ENST00000454784.9:n.2443-427_2443-426del
NM_173600.2:c.2397-427_2397-426del	NP_775871.2:n.2397-427_2397-426del
XR_944866.1:n.75-8805_75-8804del
XR_944867.1:n.75-8805_75-8804del
XR_944868.1:n.75-8805_75-8804del
XR_944869.1:n.75-8805_75-8804del
XR_944870.1:n.75-8805_75-8804del
XR_944871.1:n.75-8805_75-8804del
XR_944872.1:n.81-8805_81-8804del
XR_944873.1:n.75-8805_75-8804del
XR_001749087.1:n.75-8805_75-8804del
XR_001749088.1:n.75-8805_75-8804del
XR_944868.2:n.75-8805_75-8804del
XR_944869.2:n.75-8805_75-8804del