Canonical Allele Identifier: CA500206223

Gene: KRT16

Linked Data

• COSMIC: COSM329674
• MyVariant Identifiers: chr17:g.39768708del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612457del , CM000679.2:g.41612457del	GRCh38
NC_000017.10:g.39768709del , CM000679.1:g.39768709del	GRCh37
NC_000017.9:g.37022235del	NCBI36
NG_008301.1:g.5373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.234del MANE Select	ENSP00000301653.3:p.Phe78LeufsTer?
ENST00000301653.8:c.234del	ENSP00000301653.3:p.Phe78LeufsTer?
ENST00000588319.1:n.311del
ENST00000593067.1:c.-312-169del	ENSP00000467124.1:n.-312-169del
NM_005557.3:c.234del	NP_005548.2:p.Phe78LeufsTer?
NM_005557.4:c.234del MANE Select	NP_005548.2:p.Phe78LeufsTer?