Canonical Allele Identifier: CA2637834390
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41583202-G-GC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583202_41583203insC , CM000679.2:g.41583202_41583203insC GRCh38
NC_000017.10:g.39739454_39739455insC , CM000679.1:g.39739454_39739455insC GRCh37
NC_000017.9:g.36992980_36992981insC NCBI36
NG_008624.1:g.8693_8694insG

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+32_1274+33insG MANE Select ENSP00000167586.6:n.1274+32_1274+33insG
ENST00000167586.6:c.1274+32_1274+33insG ENSP00000167586.6:n.1274+32_1274+33insG
ENST00000441550.2:n.221+32_221+33insG
NM_000526.4:c.1274+32_1274+33insG NP_000517.2:n.1274+32_1274+33insG
NM_000526.5:c.1274+32_1274+33insG MANE Select NP_000517.3:n.1274+32_1274+33insG
Search 100 bp 5'
Search 100 bp 3'