Canonical Allele Identifier: CA2563411157
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583515_41583518del , CM000679.2:g.41583515_41583518del GRCh38
NC_000017.10:g.39739767_39739770del , CM000679.1:g.39739767_39739770del GRCh37
NC_000017.9:g.36993293_36993296del NCBI36
NG_008624.1:g.8378_8381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1053+33_1053+36del MANE Select ENSP00000167586.6:n.1053+33_1053+36del
ENST00000167586.6:c.1053+33_1053+36del ENSP00000167586.6:n.1053+33_1053+36del
ENST00000476662.1:n.503+33_503+36del
NM_000526.4:c.1053+33_1053+36del NP_000517.2:n.1053+33_1053+36del
NM_000526.5:c.1053+33_1053+36del MANE Select NP_000517.3:n.1053+33_1053+36del
Search 100 bp 5'
Search 100 bp 3'