Canonical Allele Identifier: CA399483905
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1318809672
gnomAD v2: 17-39743043-T-C
gnomAD v3: 17-41586791-T-C
gnomAD v4: 17-41586791-T-C
MyVariant Identifiers: chr17:g.39743043T>C (hg19) chr17:g.41586791T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586791T>C , CM000679.2:g.41586791T>C GRCh38
NC_000017.10:g.39743043T>C , CM000679.1:g.39743043T>C GRCh37
NC_000017.9:g.36996569T>C NCBI36
NG_008624.1:g.5105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.44A>G MANE Select ENSP00000167586.6:p.Lys15Arg
ENST00000167586.6:c.44A>G ENSP00000167586.6:p.Lys15Arg
NM_000526.4:c.44A>G NP_000517.2:p.Lys15Arg
NM_000526.5:c.44A>G MANE Select NP_000517.3:p.Lys15Arg
Search 100 bp 5'
Search 100 bp 3'