Canonical Allele Identifier: CA399476652
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583620C>A , CM000679.2:g.41583620C>A GRCh38
NC_000017.10:g.39739872C>A , CM000679.1:g.39739872C>A GRCh37
NC_000017.9:g.36993398C>A NCBI36
NG_008624.1:g.8276G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.984G>T MANE Select ENSP00000167586.6:p.Lys328Asn
ENST00000167586.6:c.984G>T ENSP00000167586.6:p.Lys328Asn
ENST00000476662.1:n.434G>T
NM_000526.4:c.984G>T NP_000517.2:p.Lys328Asn
NM_000526.5:c.984G>T MANE Select NP_000517.3:p.Lys328Asn