Canonical Allele Identifier: CA399474972
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583121A>G , CM000679.2:g.41583121A>G GRCh38
NC_000017.10:g.39739373A>G , CM000679.1:g.39739373A>G GRCh37
NC_000017.9:g.36992899A>G NCBI36
NG_008624.1:g.8775T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1294T>C MANE Select ENSP00000167586.6:p.Ser432Pro
ENST00000167586.6:c.1294T>C ENSP00000167586.6:p.Ser432Pro
ENST00000441550.2:n.241T>C
NM_000526.4:c.1294T>C NP_000517.2:p.Ser432Pro
NM_000526.5:c.1294T>C MANE Select NP_000517.3:p.Ser432Pro