Canonical Allele Identifier: CA983757285
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1312949182
gnomAD v3: 17-41583202-G-GA
gnomAD v4: 17-41583202-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583202_41583203insA , CM000679.2:g.41583202_41583203insA GRCh38
NC_000017.10:g.39739454_39739455insA , CM000679.1:g.39739454_39739455insA GRCh37
NC_000017.9:g.36992980_36992981insA NCBI36
NG_008624.1:g.8693_8694insT

Transcript Alleles

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