Canonical Allele Identifier: CA216992
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66383
ClinVar RCV Id: RCV000056758
dbSNP Id: rs113582618
COSMIC: COSM211466
MyVariant Identifiers: chr17:g.39740011C>T (hg19) chr17:g.41583759C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583759C>T , CM000679.2:g.41583759C>T GRCh38
NC_000017.10:g.39740011C>T , CM000679.1:g.39740011C>T GRCh37
NC_000017.9:g.36993537C>T NCBI36
NG_008624.1:g.8137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.927+1G>A MANE Select ENSP00000167586.6:n.927+1G>A
ENST00000167586.6:c.927+1G>A ENSP00000167586.6:n.927+1G>A
ENST00000476662.1:n.377+1G>A
NM_000526.4:c.927+1G>A NP_000517.2:n.927+1G>A
NM_000526.5:c.927+1G>A MANE Select NP_000517.3:n.927+1G>A
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