Canonical Allele Identifier: CA216923
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66348
ClinVar RCV Id: RCV000056719
dbSNP Id: rs58330629
MyVariant Identifiers: chr17:g.39742713C>G (hg19) chr17:g.41586461C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586461C>G , CM000679.2:g.41586461C>G GRCh38
NC_000017.10:g.39742713C>G , CM000679.1:g.39742713C>G GRCh37
NC_000017.9:g.36996239C>G NCBI36
NG_008624.1:g.5435G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.374G>C MANE Select ENSP00000167586.6:p.Arg125Pro
ENST00000167586.6:c.374G>C ENSP00000167586.6:p.Arg125Pro
NM_000526.4:c.374G>C NP_000517.2:p.Arg125Pro
NM_000526.5:c.374G>C MANE Select NP_000517.3:p.Arg125Pro
Search 100 bp 5'
Search 100 bp 3'