Canonical Allele Identifier: CA500205800
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586718-G-C
MyVariant Identifiers: chr17:g.39742970G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586718G>C , CM000679.2:g.41586718G>C GRCh38
NC_000017.10:g.39742970G>C , CM000679.1:g.39742970G>C GRCh37
NC_000017.9:g.36996496G>C NCBI36
NG_008624.1:g.5178C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.117C>G MANE Select ENSP00000167586.6:p.Ser39=
ENST00000167586.6:c.117C>G ENSP00000167586.6:p.Ser39=
NM_000526.4:c.117C>G NP_000517.2:p.Ser39=
NM_000526.5:c.117C>G MANE Select NP_000517.3:p.Ser39=
Search 100 bp 5'
Search 100 bp 3'