Canonical Allele Identifier: CA399477121
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583780C>A , CM000679.2:g.41583780C>A GRCh38
NC_000017.10:g.39740032C>A , CM000679.1:g.39740032C>A GRCh37
NC_000017.9:g.36993558C>A NCBI36
NG_008624.1:g.8116G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.907G>T MANE Select ENSP00000167586.6:p.Glu303Ter
ENST00000167586.6:c.907G>T ENSP00000167586.6:p.Glu303Ter
ENST00000476662.1:n.357G>T
NM_000526.4:c.907G>T NP_000517.2:p.Glu303Ter
NM_000526.5:c.907G>T MANE Select NP_000517.3:p.Glu303Ter