Canonical Allele Identifier: CA2843632367

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586634del , CM000679.2:g.41586634del	GRCh38
NC_000017.10:g.39742886del , CM000679.1:g.39742886del	GRCh37
NC_000017.9:g.36996412del	NCBI36
NG_008624.1:g.5262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.201del MANE Select	ENSP00000167586.6:p.Gly68AlafsTer?
ENST00000167586.6:c.201del	ENSP00000167586.6:p.Gly68AlafsTer?
NM_000526.4:c.201del	NP_000517.2:p.Gly68AlafsTer?
NM_000526.5:c.201del MANE Select	NP_000517.3:p.Gly68AlafsTer?