Canonical Allele Identifier: CA2809495801
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583457_41583551del , CM000679.2:g.41583457_41583551del GRCh38
NC_000017.10:g.39739709_39739803del , CM000679.1:g.39739709_39739803del GRCh37
NC_000017.9:g.36993235_36993329del NCBI36
NG_008624.1:g.8346_8440del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1053+1_1054-1del
ENST00000167586.6:c.1053+1_1054-1del
ENST00000476662.1:n.503+1_504-1del
NM_000526.4:c.1053+1_1054-1del
NM_000526.5:c.1053+1_1054-1del