Canonical Allele Identifier: CA399483661
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39743013C>G (hg19) chr17:g.41586761C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586761C>G , CM000679.2:g.41586761C>G GRCh38
NC_000017.10:g.39743013C>G , CM000679.1:g.39743013C>G GRCh37
NC_000017.9:g.36996539C>G NCBI36
NG_008624.1:g.5135G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.74G>C MANE Select ENSP00000167586.6:p.Gly25Ala
ENST00000167586.6:c.74G>C ENSP00000167586.6:p.Gly25Ala
NM_000526.4:c.74G>C NP_000517.2:p.Gly25Ala
NM_000526.5:c.74G>C MANE Select NP_000517.3:p.Gly25Ala
Search 100 bp 5'
Search 100 bp 3'