Canonical Allele Identifier: CA500205448
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739507C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583255C>G , CM000679.2:g.41583255C>G GRCh38
NC_000017.10:g.39739507C>G , CM000679.1:g.39739507C>G GRCh37
NC_000017.9:g.36993033C>G NCBI36
NG_008624.1:g.8641G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1254G>C MANE Select ENSP00000167586.6:p.Leu418=
ENST00000167586.6:c.1254G>C ENSP00000167586.6:p.Leu418=
ENST00000441550.2:n.201G>C
ENST00000476662.1:n.704G>C
NM_000526.4:c.1254G>C NP_000517.2:p.Leu418=
NM_000526.5:c.1254G>C MANE Select NP_000517.3:p.Leu418=