Canonical Allele Identifier: CA235400697

Gene: MUC19

Linked Data

• dbSNP Id: rs35642223
• MyVariant Identifiers: chr12:g.40823038_40823039insG (hg19) ; chr12:g.40429236_40429237insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40429238dup , CM000674.2:g.40429238dup	GRCh38
NC_000012.11:g.40823040dup , CM000674.1:g.40823040dup	GRCh37
NC_000012.10:g.39109307dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454784.10:c.2397-304dup	ENSP00000508949.1:n.2397-304dup
ENST00000454784.9:n.2443-304dup
NM_173600.2:c.2397-304dup	NP_775871.2:n.2397-304dup
XR_944866.1:n.75-8926dup
XR_944867.1:n.75-8926dup
XR_944868.1:n.75-8926dup
XR_944869.1:n.75-8926dup
XR_944870.1:n.75-8926dup
XR_944871.1:n.75-8926dup
XR_944872.1:n.81-8926dup
XR_944873.1:n.75-8926dup
XR_001749087.1:n.75-8926dup
XR_001749088.1:n.75-8926dup
XR_944868.2:n.75-8926dup
XR_944869.2:n.75-8926dup