Canonical Allele Identifier: CA2260086797
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586408G= , CM000679.2:g.41586408G= GRCh38
NC_000017.10:g.39742660G= , CM000679.1:g.39742660G= GRCh37
NC_000017.9:g.36996186G= NCBI36
NG_008624.1:g.5488C=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.427C= MANE Select ENSP00000167586.6:p.Leu143=
ENST00000167586.6:c.427C= ENSP00000167586.6:p.Leu143=
NM_000526.4:c.427C= NP_000517.2:p.Leu143=
NM_000526.5:c.427C= MANE Select NP_000517.3:p.Leu143=