Canonical Allele Identifier: CA626215410
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1312949182
gnomAD v2: 17-39739454-G-GT
gnomAD v3: 17-41583202-G-GT
gnomAD v4: 17-41583202-G-GT
MyVariant Identifiers: chr17:g.39739454_39739455insT (hg19) chr17:g.41583202_41583203insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583202_41583203insT , CM000679.2:g.41583202_41583203insT GRCh38
NC_000017.10:g.39739454_39739455insT , CM000679.1:g.39739454_39739455insT GRCh37
NC_000017.9:g.36992980_36992981insT NCBI36
NG_008624.1:g.8693_8694insA

Transcript Alleles

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