Canonical Allele Identifier: CA8562850
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs542727743
ExAC: 17:39743108 C / T
gnomAD v2: 17-39743108-C-T
gnomAD v3: 17-41586856-C-T
gnomAD v4: 17-41586856-C-T
MyVariant Identifiers: chr17:g.39743108C>T (hg19) chr17:g.41586856C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586856C>T , CM000679.2:g.41586856C>T GRCh38
NC_000017.10:g.39743108C>T , CM000679.1:g.39743108C>T GRCh37
NC_000017.9:g.36996634C>T NCBI36
NG_008624.1:g.5040G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-22G>A MANE Select ENSP00000167586.6:n.-22G>A
ENST00000167586.6:c.-22G>A ENSP00000167586.6:n.-22G>A
NM_000526.4:c.-22G>A NP_000517.2:n.-22G>A
NM_000526.5:c.-22G>A MANE Select NP_000517.3:n.-22G>A
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