Canonical Allele Identifier: CA2260085351
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583327_41583328delinsCT , CM000679.2:g.41583327_41583328delinsCT GRCh38
NC_000017.10:g.39739579_39739580delinsCT , CM000679.1:g.39739579_39739580delinsCT GRCh37
NC_000017.9:g.36993105_36993106delinsCT NCBI36
NG_008624.1:g.8568_8569delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1181_1182delinsAG MANE Select ENSP00000167586.6:p.Gln394=
ENST00000167586.6:c.1181_1182delinsAG ENSP00000167586.6:p.Gln394=
ENST00000441550.2:n.128_129delinsAG
ENST00000476662.1:n.631_632delinsAG
NM_000526.4:c.1181_1182delinsAG NP_000517.2:p.Gln394=
NM_000526.5:c.1181_1182delinsAG MANE Select NP_000517.3:p.Gln394=
Search 100 bp 5'
Search 100 bp 3'