Canonical Allele Identifier: CA216915
Community Standard Title: NM_000526.5(KRT14):c.369T>C (p.Asn123=)
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586466A>G , CM000679.2:g.41586466A>G GRCh38
NC_000017.10:g.39742718A>G , CM000679.1:g.39742718A>G GRCh37
NC_000017.9:g.36996244A>G NCBI36
NG_008624.1:g.5430T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000526.5:c.369T>C MANE Select NP_000517.3:p.Asn123=
ENST00000167586.7:c.369T>C MANE Select ENSP00000167586.6:p.Asn123=
NM_000526.4:c.369T>C NP_000517.2:p.Asn123=
ENST00000167586.6:c.369T>C ENSP00000167586.6:p.Asn123=
Search 100 bp 5'
Search 100 bp 3'