Canonical Allele Identifier: CA8562698
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs773186304
ExAC: 17:39742534 T / C
gnomAD v2: 17-39742534-T-C
gnomAD v4: 17-41586282-T-C
MyVariant Identifiers: chr17:g.39742534T>C (hg19) chr17:g.41586282T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586282T>C , CM000679.2:g.41586282T>C GRCh38
NC_000017.10:g.39742534T>C , CM000679.1:g.39742534T>C GRCh37
NC_000017.9:g.36996060T>C NCBI36
NG_008624.1:g.5614A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+28A>G MANE Select ENSP00000167586.6:n.525+28A>G
ENST00000167586.6:c.525+28A>G ENSP00000167586.6:n.525+28A>G
NM_000526.4:c.525+28A>G NP_000517.2:n.525+28A>G
NM_000526.5:c.525+28A>G MANE Select NP_000517.3:n.525+28A>G
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