Canonical Allele Identifier: CA2559752918
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583721_41583725del , CM000679.2:g.41583721_41583725del GRCh38
NC_000017.10:g.39739973_39739977del , CM000679.1:g.39739973_39739977del GRCh37
NC_000017.9:g.36993499_36993503del NCBI36
NG_008624.1:g.8171_8175del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+35_927+39del MANE Select ENSP00000167586.6:n.927+35_927+39del
ENST00000167586.6:c.927+35_927+39del ENSP00000167586.6:n.927+35_927+39del
ENST00000476662.1:n.377+35_377+39del
NM_000526.4:c.927+35_927+39del NP_000517.2:n.927+35_927+39del
NM_000526.5:c.927+35_927+39del MANE Select NP_000517.3:n.927+35_927+39del