Canonical Allele Identifier: CA2637837222
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586282-T-G
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Genomic Alleles

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

Transcript Alleles

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