Canonical Allele Identifier: CA500205426
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739926T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583674T>A , CM000679.2:g.41583674T>A GRCh38
NC_000017.10:g.39739926T>A , CM000679.1:g.39739926T>A GRCh37
NC_000017.9:g.36993452T>A NCBI36
NG_008624.1:g.8222A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.930A>T MANE Select ENSP00000167586.6:p.Thr310=
ENST00000167586.6:c.930A>T ENSP00000167586.6:p.Thr310=
ENST00000476662.1:n.380A>T
NM_000526.4:c.930A>T NP_000517.2:p.Thr310=
NM_000526.5:c.930A>T MANE Select NP_000517.3:p.Thr310=