Canonical Allele Identifier: CA499992011
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39742742C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586490C>T , CM000679.2:g.41586490C>T GRCh38
NC_000017.10:g.39742742C>T , CM000679.1:g.39742742C>T GRCh37
NC_000017.9:g.36996268C>T NCBI36
NG_008624.1:g.5406G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.345G>A MANE Select ENSP00000167586.6:p.Glu115=
ENST00000167586.6:c.345G>A ENSP00000167586.6:p.Glu115=
NM_000526.4:c.345G>A NP_000517.2:p.Glu115=
NM_000526.5:c.345G>A MANE Select NP_000517.3:p.Glu115=