Canonical Allele Identifier: CA399483655
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586759-C-T
MyVariant Identifiers: chr17:g.39743011C>T (hg19) chr17:g.41586759C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586759C>T , CM000679.2:g.41586759C>T GRCh38
NC_000017.10:g.39743011C>T , CM000679.1:g.39743011C>T GRCh37
NC_000017.9:g.36996537C>T NCBI36
NG_008624.1:g.5137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.76G>A MANE Select ENSP00000167586.6:p.Gly26Ser
ENST00000167586.6:c.76G>A ENSP00000167586.6:p.Gly26Ser
NM_000526.4:c.76G>A NP_000517.2:p.Gly26Ser
NM_000526.5:c.76G>A MANE Select NP_000517.3:p.Gly26Ser
Search 100 bp 5'
Search 100 bp 3'