Canonical Allele Identifier: CA2260085276
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs776207059
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583203_41583204insA , CM000679.2:g.41583203_41583204insA GRCh38
NC_000017.10:g.39739455_39739456insA , CM000679.1:g.39739455_39739456insA GRCh37
NC_000017.9:g.36992981_36992982insA NCBI36
NG_008624.1:g.8692_8693insT

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+31_1274+32insT MANE Select ENSP00000167586.6:n.1274+31_1274+32insT
ENST00000167586.6:c.1274+31_1274+32insT ENSP00000167586.6:n.1274+31_1274+32insT
ENST00000441550.2:n.221+31_221+32insT
NM_000526.4:c.1274+31_1274+32insT NP_000517.2:n.1274+31_1274+32insT
NM_000526.5:c.1274+31_1274+32insT MANE Select NP_000517.3:n.1274+31_1274+32insT
Search 100 bp 5'
Search 100 bp 3'