Canonical Allele Identifier: CA290665664
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs11551748
gnomAD v2: 17-39742985-G-A
gnomAD v4: 17-41586733-G-A
MyVariant Identifiers: chr17:g.39742985G>A (hg19) chr17:g.41586733G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586733G>A , CM000679.2:g.41586733G>A GRCh38
NC_000017.10:g.39742985G>A , CM000679.1:g.39742985G>A GRCh37
NC_000017.9:g.36996511G>A NCBI36
NG_008624.1:g.5163C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.102C>T MANE Select ENSP00000167586.6:p.Val34=
ENST00000167586.6:c.102C>T ENSP00000167586.6:p.Val34=
NM_000526.4:c.102C>T NP_000517.2:p.Val34=
NM_000526.5:c.102C>T MANE Select NP_000517.3:p.Val34=
Search 100 bp 5'
Search 100 bp 3'