Canonical Allele Identifier: CA399482564
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586474T>G , CM000679.2:g.41586474T>G GRCh38
NC_000017.10:g.39742726T>G , CM000679.1:g.39742726T>G GRCh37
NC_000017.9:g.36996252T>G NCBI36
NG_008624.1:g.5422A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.361A>C MANE Select ENSP00000167586.6:p.Asn121His
ENST00000167586.6:c.361A>C ENSP00000167586.6:p.Asn121His
NM_000526.4:c.361A>C NP_000517.2:p.Asn121His
NM_000526.5:c.361A>C MANE Select NP_000517.3:p.Asn121His