Canonical Allele Identifier: CA399477615
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740128C>A (hg19) chr17:g.41583876C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583876C>A , CM000679.2:g.41583876C>A GRCh38
NC_000017.10:g.39740128C>A , CM000679.1:g.39740128C>A GRCh37
NC_000017.9:g.36993654C>A NCBI36
NG_008624.1:g.8020G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.811G>T MANE Select ENSP00000167586.6:p.Glu271Ter
ENST00000167586.6:c.811G>T ENSP00000167586.6:p.Glu271Ter
ENST00000476662.1:n.261G>T
NM_000526.4:c.811G>T NP_000517.2:p.Glu271Ter
NM_000526.5:c.811G>T MANE Select NP_000517.3:p.Glu271Ter
Search 100 bp 5'
Search 100 bp 3'