Canonical Allele Identifier: CA2637837562
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586648_41586649insTA , CM000679.2:g.41586648_41586649insTA GRCh38
NC_000017.10:g.39742900_39742901insTA , CM000679.1:g.39742900_39742901insTA GRCh37
NC_000017.9:g.36996426_36996427insTA NCBI36
NG_008624.1:g.5248_5249insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.187_188insAT MANE Select ENSP00000167586.6:p.Cys63TyrfsTer?
ENST00000167586.6:c.187_188insAT ENSP00000167586.6:p.Cys63TyrfsTer?
NM_000526.4:c.187_188insAT NP_000517.2:p.Gly64ThrfsTer?
NM_000526.5:c.187_188insAT MANE Select NP_000517.3:p.Cys63TyrfsTer?