Canonical Allele Identifier: CA2260085934
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584422_41584425delinsACCC , CM000679.2:g.41584422_41584425delinsACCC GRCh38
NC_000017.10:g.39740674_39740677delinsACCC , CM000679.1:g.39740674_39740677delinsACCC GRCh37
NC_000017.9:g.36994200_36994203delinsACCC NCBI36
NG_008624.1:g.7471_7474delinsGGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-12_609-9delinsGGGT MANE Select ENSP00000167586.6:n.609-12_609-9delinsGGG...
ENST00000167586.6:c.609-12_609-9delinsGGGT ENSP00000167586.6:n.609-12_609-9delinsGGG...
ENST00000476662.1:n.47_50delinsGGGT
NM_000526.4:c.609-12_609-9delinsGGGT NP_000517.2:n.609-12_609-9delinsGGGT
NM_000526.5:c.609-12_609-9delinsGGGT MANE Select NP_000517.3:n.609-12_609-9delinsGGGT