Canonical Allele Identifier: CA2260085218
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583110_41583121delinsCGATCCAGAGGA , CM000679.2:g.41583110_41583121delinsCGATCCAGAGGA GRCh38
NC_000017.10:g.39739362_39739373delinsCGATCCAGAGGA , CM000679.1:g.39739362_39739373delinsCGATCCAGAGGA GRCh37
NC_000017.9:g.36992888_36992899delinsCGATCCAGAGGA NCBI36
NG_008624.1:g.8775_8786delinsTCCTCTGGATCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1294_1305delinsTCCTCTGGATCG MANE Select ENSP00000167586.6:p.Ser432=
ENST00000167586.6:c.1294_1305delinsTCCTCTGGATCG ENSP00000167586.6:p.Ser432=
ENST00000441550.2:n.241_252delinsTCCTCTGGATCG
NM_000526.4:c.1294_1305delinsTCCTCTGGATCG NP_000517.2:p.Ser432=
NM_000526.5:c.1294_1305delinsTCCTCTGGATCG MANE Select NP_000517.3:p.Ser432=
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