Canonical Allele Identifier: CA399483642
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586755-C-T
MyVariant Identifiers: chr17:g.39743007C>T (hg19) chr17:g.41586755C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586755C>T , CM000679.2:g.41586755C>T GRCh38
NC_000017.10:g.39743007C>T , CM000679.1:g.39743007C>T GRCh37
NC_000017.9:g.36996533C>T NCBI36
NG_008624.1:g.5141G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.80G>A MANE Select ENSP00000167586.6:p.Gly27Asp
ENST00000167586.6:c.80G>A ENSP00000167586.6:p.Gly27Asp
NM_000526.4:c.80G>A NP_000517.2:p.Gly27Asp
NM_000526.5:c.80G>A MANE Select NP_000517.3:p.Gly27Asp
Search 100 bp 5'
Search 100 bp 3'