Canonical Allele Identifier: CA2260085140
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1019991995
gnomAD v4: 17-41583012-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583012G>T , CM000679.2:g.41583012G>T GRCh38
NC_000017.10:g.39739264G>T , CM000679.1:g.39739264G>T GRCh37
NC_000017.9:g.36992790G>T NCBI36
NG_008624.1:g.8884C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+82C>A MANE Select ENSP00000167586.6:n.1321+82C>A
ENST00000167586.6:c.1321+82C>A ENSP00000167586.6:n.1321+82C>A
ENST00000441550.2:n.350C>A
NM_000526.4:c.1321+82C>A NP_000517.2:n.1321+82C>A
NM_000526.5:c.1321+82C>A MANE Select NP_000517.3:n.1321+82C>A
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