Canonical Allele Identifier: CA2260085429
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907409741
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583504C>T , CM000679.2:g.41583504C>T GRCh38
NC_000017.10:g.39739756C>T , CM000679.1:g.39739756C>T GRCh37
NC_000017.9:g.36993282C>T NCBI36
NG_008624.1:g.8392G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1053+47G>A MANE Select ENSP00000167586.6:n.1053+47G>A
ENST00000167586.6:c.1053+47G>A ENSP00000167586.6:n.1053+47G>A
ENST00000476662.1:n.503+47G>A
NM_000526.4:c.1053+47G>A NP_000517.2:n.1053+47G>A
NM_000526.5:c.1053+47G>A MANE Select NP_000517.3:n.1053+47G>A
Search 100 bp 5'
Search 100 bp 3'