Canonical Allele Identifier: CA2260087066
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586834_41586835delinsTG , CM000679.2:g.41586834_41586835delinsTG GRCh38
NC_000017.10:g.39743086_39743087delinsTG , CM000679.1:g.39743086_39743087delinsTG GRCh37
NC_000017.9:g.36996612_36996613delinsTG NCBI36
NG_008624.1:g.5061_5062delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-1_1delinsCA
ENST00000167586.6:c.-1_1delinsCA
NM_000526.4:c.-1_1delinsCA
NM_000526.5:c.-1_1delinsCA