Canonical Allele Identifier: CA772039845
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1279680138
MyVariant Identifiers: chr17:g.39740676C>T (hg19) chr17:g.41584424C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584424C>T , CM000679.2:g.41584424C>T GRCh38
NC_000017.10:g.39740676C>T , CM000679.1:g.39740676C>T GRCh37
NC_000017.9:g.36994202C>T NCBI36
NG_008624.1:g.7472G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-11G>A MANE Select ENSP00000167586.6:n.609-11G>A
ENST00000167586.6:c.609-11G>A ENSP00000167586.6:n.609-11G>A
ENST00000476662.1:n.48G>A
NM_000526.4:c.609-11G>A NP_000517.2:n.609-11G>A
NM_000526.5:c.609-11G>A MANE Select NP_000517.3:n.609-11G>A
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