Canonical Allele Identifier: CA2518326452
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583378_41583379insCTG , CM000679.2:g.41583378_41583379insCTG GRCh38
NC_000017.10:g.39739630_39739631insCTG , CM000679.1:g.39739630_39739631insCTG GRCh37
NC_000017.9:g.36993156_36993157insCTG NCBI36
NG_008624.1:g.8517_8518insCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1130_1131insCAG MANE Select ENSP00000167586.6:p.Ile377_Gly378insSer
ENST00000167586.6:c.1130_1131insCAG ENSP00000167586.6:p.Ile377_Gly378insSer
ENST00000441550.2:n.77_78insCAG
ENST00000476662.1:n.580_581insCAG
NM_000526.4:c.1130_1131insCAG NP_000517.2:p.Ile377_Gly378insSer
NM_000526.5:c.1130_1131insCAG MANE Select NP_000517.3:p.Ile377_Gly378insSer
Search 100 bp 5'
Search 100 bp 3'