Canonical Allele Identifier: CA2576267619
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583736C>T , CM000679.2:g.41583736C>T GRCh38
NC_000017.10:g.39739988C>T , CM000679.1:g.39739988C>T GRCh37
NC_000017.9:g.36993514C>T NCBI36
NG_008624.1:g.8160G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+24G>A MANE Select ENSP00000167586.6:n.927+24G>A
ENST00000167586.6:c.927+24G>A ENSP00000167586.6:n.927+24G>A
ENST00000476662.1:n.377+24G>A
NM_000526.4:c.927+24G>A NP_000517.2:n.927+24G>A
NM_000526.5:c.927+24G>A MANE Select NP_000517.3:n.927+24G>A
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