Canonical Allele Identifier: CA399475282
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583257G>T , CM000679.2:g.41583257G>T GRCh38
NC_000017.10:g.39739509G>T , CM000679.1:g.39739509G>T GRCh37
NC_000017.9:g.36993035G>T NCBI36
NG_008624.1:g.8639C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1252C>A MANE Select ENSP00000167586.6:p.Leu418Met
ENST00000167586.6:c.1252C>A ENSP00000167586.6:p.Leu418Met
ENST00000441550.2:n.199C>A
ENST00000476662.1:n.702C>A
NM_000526.4:c.1252C>A NP_000517.2:p.Leu418Met
NM_000526.5:c.1252C>A MANE Select NP_000517.3:p.Leu418Met