Canonical Allele Identifier: CA2809495485

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586645_41586646insAT , CM000679.2:g.41586645_41586646insAT	GRCh38
NC_000017.10:g.39742897_39742898insAT , CM000679.1:g.39742897_39742898insAT	GRCh37
NC_000017.9:g.36996423_36996424insAT	NCBI36
NG_008624.1:g.5250_5251insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.189_190insAT MANE Select	ENSP00000167586.6:p.Gly64MetfsTer?
ENST00000167586.6:c.189_190insAT	ENSP00000167586.6:p.Gly64MetfsTer?
NM_000526.4:c.189_190insAT	NP_000517.2:p.Gly64MetfsTer?
NM_000526.5:c.189_190insAT MANE Select	NP_000517.3:p.Gly64MetfsTer?