Canonical Allele Identifier: CA2535653071

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583703_41583704insGTCA , CM000679.2:g.41583703_41583704insGTCA	GRCh38
NC_000017.10:g.39739955_39739956insGTCA , CM000679.1:g.39739955_39739956insGTCA	GRCh37
NC_000017.9:g.36993481_36993482insGTCA	NCBI36
NG_008624.1:g.8192_8193insTGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.928-28_928-27insTGAC MANE Select	ENSP00000167586.6:n.928-28_928-27insTGAC
ENST00000167586.6:c.928-28_928-27insTGAC	ENSP00000167586.6:n.928-28_928-27insTGAC
ENST00000476662.1:n.378-28_378-27insTGAC
NM_000526.4:c.928-28_928-27insTGAC	NP_000517.2:n.928-28_928-27insTGAC
NM_000526.5:c.928-28_928-27insTGAC MANE Select	NP_000517.3:n.928-28_928-27insTGAC