Canonical Allele Identifier: CA2576267788
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586296G>A , CM000679.2:g.41586296G>A GRCh38
NC_000017.10:g.39742548G>A , CM000679.1:g.39742548G>A GRCh37
NC_000017.9:g.36996074G>A NCBI36
NG_008624.1:g.5600C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+14C>T MANE Select ENSP00000167586.6:n.525+14C>T
ENST00000167586.6:c.525+14C>T ENSP00000167586.6:n.525+14C>T
NM_000526.4:c.525+14C>T NP_000517.2:n.525+14C>T
NM_000526.5:c.525+14C>T MANE Select NP_000517.3:n.525+14C>T
Search 100 bp 5'
Search 100 bp 3'