Canonical Allele Identifier: CA2637834672
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583535del , CM000679.2:g.41583535del GRCh38
NC_000017.10:g.39739787del , CM000679.1:g.39739787del GRCh37
NC_000017.9:g.36993313del NCBI36
NG_008624.1:g.8362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1053+17del MANE Select ENSP00000167586.6:n.1053+17del
ENST00000167586.6:c.1053+17del ENSP00000167586.6:n.1053+17del
ENST00000476662.1:n.503+17del
NM_000526.4:c.1053+17del NP_000517.2:n.1053+17del
NM_000526.5:c.1053+17del MANE Select NP_000517.3:n.1053+17del