Canonical Allele Identifier: CA500205105
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739383G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583131G>T , CM000679.2:g.41583131G>T GRCh38
NC_000017.10:g.39739383G>T , CM000679.1:g.39739383G>T GRCh37
NC_000017.9:g.36992909G>T NCBI36
NG_008624.1:g.8765C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1284C>A MANE Select ENSP00000167586.6:p.Ser428=
ENST00000167586.6:c.1284C>A ENSP00000167586.6:p.Ser428=
ENST00000441550.2:n.231C>A
NM_000526.4:c.1284C>A NP_000517.2:p.Ser428=
NM_000526.5:c.1284C>A MANE Select NP_000517.3:p.Ser428=
Search 100 bp 5'
Search 100 bp 3'