Canonical Allele Identifier: CA8562564
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs376925607

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583687G>T , CM000679.2:g.41583687G>T GRCh38
NC_000017.10:g.39739939G>T , CM000679.1:g.39739939G>T GRCh37
NC_000017.9:g.36993465G>T NCBI36
NG_008624.1:g.8209C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-11C>A MANE Select ENSP00000167586.6:n.928-11C>A
ENST00000167586.6:c.928-11C>A ENSP00000167586.6:n.928-11C>A
ENST00000476662.1:n.378-11C>A
NM_000526.4:c.928-11C>A NP_000517.2:n.928-11C>A
NM_000526.5:c.928-11C>A MANE Select NP_000517.3:n.928-11C>A