Canonical Allele Identifier: CA399477198
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583794T>C , CM000679.2:g.41583794T>C GRCh38
NC_000017.10:g.39740046T>C , CM000679.1:g.39740046T>C GRCh37
NC_000017.9:g.36993572T>C NCBI36
NG_008624.1:g.8102A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.893A>G MANE Select ENSP00000167586.6:p.Asn298Ser
ENST00000167586.6:c.893A>G ENSP00000167586.6:p.Asn298Ser
ENST00000476662.1:n.343A>G
NM_000526.4:c.893A>G NP_000517.2:p.Asn298Ser
NM_000526.5:c.893A>G MANE Select NP_000517.3:p.Asn298Ser