Canonical Allele Identifier: CA2637837928
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586856-C-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-22G>T MANE Select ENSP00000167586.6:n.-22G>T
ENST00000167586.6:c.-22G>T ENSP00000167586.6:n.-22G>T
NM_000526.4:c.-22G>T NP_000517.2:n.-22G>T
NM_000526.5:c.-22G>T MANE Select NP_000517.3:n.-22G>T
Search 100 bp 5'
Search 100 bp 3'