Canonical Allele Identifier: CA2637834317
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41583184-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583184G>C , CM000679.2:g.41583184G>C GRCh38
NC_000017.10:g.39739436G>C , CM000679.1:g.39739436G>C GRCh37
NC_000017.9:g.36992962G>C NCBI36
NG_008624.1:g.8712C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1275-44C>G MANE Select ENSP00000167586.6:n.1275-44C>G
ENST00000167586.6:c.1275-44C>G ENSP00000167586.6:n.1275-44C>G
ENST00000441550.2:n.222-44C>G
NM_000526.4:c.1275-44C>G NP_000517.2:n.1275-44C>G
NM_000526.5:c.1275-44C>G MANE Select NP_000517.3:n.1275-44C>G
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