Canonical Allele Identifier: CA8562446
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs779312134
ExAC: 17:39739454 G / C
gnomAD v2: 17-39739454-G-C
gnomAD v3: 17-41583202-G-C
gnomAD v4: 17-41583202-G-C
MyVariant Identifiers: chr17:g.39739454G>C (hg19) chr17:g.41583202G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583202G>C , CM000679.2:g.41583202G>C GRCh38
NC_000017.10:g.39739454G>C , CM000679.1:g.39739454G>C GRCh37
NC_000017.9:g.36992980G>C NCBI36
NG_008624.1:g.8694C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1274+33C>G MANE Select ENSP00000167586.6:n.1274+33C>G
ENST00000167586.6:c.1274+33C>G ENSP00000167586.6:n.1274+33C>G
ENST00000441550.2:n.221+33C>G
NM_000526.4:c.1274+33C>G NP_000517.2:n.1274+33C>G
NM_000526.5:c.1274+33C>G MANE Select NP_000517.3:n.1274+33C>G
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