Canonical Allele Identifier: CA399475279
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583256A>G , CM000679.2:g.41583256A>G GRCh38
NC_000017.10:g.39739508A>G , CM000679.1:g.39739508A>G GRCh37
NC_000017.9:g.36993034A>G NCBI36
NG_008624.1:g.8640T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1253T>C MANE Select ENSP00000167586.6:p.Leu418Pro
ENST00000167586.6:c.1253T>C ENSP00000167586.6:p.Leu418Pro
ENST00000441550.2:n.200T>C
ENST00000476662.1:n.703T>C
NM_000526.4:c.1253T>C NP_000517.2:p.Leu418Pro
NM_000526.5:c.1253T>C MANE Select NP_000517.3:p.Leu418Pro