Canonical Allele Identifier: CA500205078
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739371G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583119G>C , CM000679.2:g.41583119G>C GRCh38
NC_000017.10:g.39739371G>C , CM000679.1:g.39739371G>C GRCh37
NC_000017.9:g.36992897G>C NCBI36
NG_008624.1:g.8777C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1296C>G MANE Select ENSP00000167586.6:p.Ser432=
ENST00000167586.6:c.1296C>G ENSP00000167586.6:p.Ser432=
ENST00000441550.2:n.243C>G
NM_000526.4:c.1296C>G NP_000517.2:p.Ser432=
NM_000526.5:c.1296C>G MANE Select NP_000517.3:p.Ser432=
Search 100 bp 5'
Search 100 bp 3'