Canonical Allele Identifier: CA500205490
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739546C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583294C>T , CM000679.2:g.41583294C>T GRCh38
NC_000017.10:g.39739546C>T , CM000679.1:g.39739546C>T GRCh37
NC_000017.9:g.36993072C>T NCBI36
NG_008624.1:g.8602G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1215G>A MANE Select ENSP00000167586.6:p.Lys405=
ENST00000167586.6:c.1215G>A ENSP00000167586.6:p.Lys405=
ENST00000441550.2:n.162G>A
ENST00000476662.1:n.665G>A
NM_000526.4:c.1215G>A NP_000517.2:p.Lys405=
NM_000526.5:c.1215G>A MANE Select NP_000517.3:p.Lys405=