Canonical Allele Identifier: CA290665529
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs111523432
MyVariant Identifiers: chr17:g.39742559C>A (hg19) chr17:g.41586307C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586307C>A , CM000679.2:g.41586307C>A GRCh38
NC_000017.10:g.39742559C>A , CM000679.1:g.39742559C>A GRCh37
NC_000017.9:g.36996085C>A NCBI36
NG_008624.1:g.5589G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+3G>T MANE Select ENSP00000167586.6:n.525+3G>T
ENST00000167586.6:c.525+3G>T ENSP00000167586.6:n.525+3G>T
NM_000526.4:c.525+3G>T NP_000517.2:n.525+3G>T
NM_000526.5:c.525+3G>T MANE Select NP_000517.3:n.525+3G>T
Search 100 bp 5'
Search 100 bp 3'