Canonical Allele Identifier: CA2637837925
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586853G>A , CM000679.2:g.41586853G>A GRCh38
NC_000017.10:g.39743105G>A , CM000679.1:g.39743105G>A GRCh37
NC_000017.9:g.36996631G>A NCBI36
NG_008624.1:g.5043C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-19C>T MANE Select ENSP00000167586.6:n.-19C>T
ENST00000167586.6:c.-19C>T ENSP00000167586.6:n.-19C>T
NM_000526.4:c.-19C>T NP_000517.2:n.-19C>T
NM_000526.5:c.-19C>T MANE Select NP_000517.3:n.-19C>T