Canonical Allele Identifier: CA2695225880

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583337_41583366del , CM000679.2:g.41583337_41583366del	GRCh38
NC_000017.10:g.39739589_39739618del , CM000679.1:g.39739589_39739618del	GRCh37
NC_000017.9:g.36993115_36993144del	NCBI36
NG_008624.1:g.8538_8567del

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1151_1180del MANE Select	ENSP00000167586.6:p.Leu384_Gln393del
ENST00000167586.6:c.1151_1180del	ENSP00000167586.6:p.Leu384_Gln393del
ENST00000441550.2:n.98_127del
ENST00000476662.1:n.601_630del
NM_000526.4:c.1151_1180del	NP_000517.2:p.Leu384_Gln393del
NM_000526.5:c.1151_1180del MANE Select	NP_000517.3:p.Leu384_Gln393del