Canonical Allele Identifier: CA399477184
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907424710
gnomAD v4: 17-41583792-G-A
MyVariant Identifiers: chr17:g.39740044G>A (hg19) chr17:g.41583792G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583792G>A , CM000679.2:g.41583792G>A GRCh38
NC_000017.10:g.39740044G>A , CM000679.1:g.39740044G>A GRCh37
NC_000017.9:g.36993570G>A NCBI36
NG_008624.1:g.8104C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.895C>T MANE Select ENSP00000167586.6:p.Arg299Cys
ENST00000167586.6:c.895C>T ENSP00000167586.6:p.Arg299Cys
ENST00000476662.1:n.345C>T
NM_000526.4:c.895C>T NP_000517.2:p.Arg299Cys
NM_000526.5:c.895C>T MANE Select NP_000517.3:p.Arg299Cys
Search 100 bp 5'
Search 100 bp 3'