Canonical Allele Identifier: CA8562699
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs746772333
ExAC: 17:39742535 G / T
gnomAD v2: 17-39742535-G-T
gnomAD v4: 17-41586283-G-T
MyVariant Identifiers: chr17:g.39742535G>T (hg19) chr17:g.41586283G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586283G>T , CM000679.2:g.41586283G>T GRCh38
NC_000017.10:g.39742535G>T , CM000679.1:g.39742535G>T GRCh37
NC_000017.9:g.36996061G>T NCBI36
NG_008624.1:g.5613C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+27C>A MANE Select ENSP00000167586.6:n.525+27C>A
ENST00000167586.6:c.525+27C>A ENSP00000167586.6:n.525+27C>A
NM_000526.4:c.525+27C>A NP_000517.2:n.525+27C>A
NM_000526.5:c.525+27C>A MANE Select NP_000517.3:n.525+27C>A
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