Canonical Allele Identifier: CA8562568
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs780098309

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583710G>A , CM000679.2:g.41583710G>A GRCh38
NC_000017.10:g.39739962G>A , CM000679.1:g.39739962G>A GRCh37
NC_000017.9:g.36993488G>A NCBI36
NG_008624.1:g.8186C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-34C>T MANE Select ENSP00000167586.6:n.928-34C>T
ENST00000167586.6:c.928-34C>T ENSP00000167586.6:n.928-34C>T
ENST00000476662.1:n.378-34C>T
NM_000526.4:c.928-34C>T NP_000517.2:n.928-34C>T
NM_000526.5:c.928-34C>T MANE Select NP_000517.3:n.928-34C>T