Canonical Allele Identifier: CA8562437
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs35380497

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583207del , CM000679.2:g.41583207del GRCh38
NC_000017.10:g.39739459del , CM000679.1:g.39739459del GRCh37
NC_000017.9:g.36992985del NCBI36
NG_008624.1:g.8696del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+35del MANE Select ENSP00000167586.6:n.1274+35del
ENST00000167586.6:c.1274+35del ENSP00000167586.6:n.1274+35del
ENST00000441550.2:n.221+35del
NM_000526.4:c.1274+35del NP_000517.2:n.1274+35del
NM_000526.5:c.1274+35del MANE Select NP_000517.3:n.1274+35del