Canonical Allele Identifier: CA2569711940
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583728_41583729insTC , CM000679.2:g.41583728_41583729insTC GRCh38
NC_000017.10:g.39739980_39739981insTC , CM000679.1:g.39739980_39739981insTC GRCh37
NC_000017.9:g.36993506_36993507insTC NCBI36
NG_008624.1:g.8167_8168insGA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+31_927+32insGA MANE Select ENSP00000167586.6:n.927+31_927+32insGA
ENST00000167586.6:c.927+31_927+32insGA ENSP00000167586.6:n.927+31_927+32insGA
ENST00000476662.1:n.377+31_377+32insGA
NM_000526.4:c.927+31_927+32insGA NP_000517.2:n.927+31_927+32insGA
NM_000526.5:c.927+31_927+32insGA MANE Select NP_000517.3:n.927+31_927+32insGA