Canonical Allele Identifier: CA290664724
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs945383360
MyVariant Identifiers: chr17:g.39739365_39739366insC (hg19) chr17:g.41583113_41583114insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583115dup , CM000679.2:g.41583115dup GRCh38
NC_000017.10:g.39739367dup , CM000679.1:g.39739367dup GRCh37
NC_000017.9:g.36992893dup NCBI36
NG_008624.1:g.8782dup

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1301dup MANE Select ENSP00000167586.6:p.Ser435IlefsTer?
ENST00000167586.6:c.1301dup ENSP00000167586.6:p.Ser435IlefsTer?
ENST00000441550.2:n.248dup
NM_000526.4:c.1301dup NP_000517.2:p.Ser435IlefsTer?
NM_000526.5:c.1301dup MANE Select NP_000517.3:p.Ser435IlefsTer?
Search 100 bp 5'
Search 100 bp 3'