Canonical Allele Identifier: CA645576831

Gene: KRT17

Linked Data

• COSMIC: COSM5645411

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624245_41624246insA , CM000679.2:g.41624245_41624246insA	GRCh38
NC_000017.10:g.39780497_39780498insA , CM000679.1:g.39780497_39780498insA	GRCh37
NC_000017.9:g.37034023_37034024insA	NCBI36
NG_008625.1:g.5385_5386insT
NG_009090.2:g.167467_167468insT , LRG_401:g.167467_167468insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.264_265insT MANE Select	ENSP00000308452.8:p.Gln89SerfsTer5
ENST00000311208.12:c.264_265insT	ENSP00000308452.8:p.Gln89SerfsTer5
ENST00000463128.5:c.-312-40_-312-39insT	ENSP00000468672.1:n.-312-40_-312-39insT
ENST00000491673.1:n.330_331insT
ENST00000493253.5:n.51_52insT
ENST00000540235.5:c.59_60insT	ENSP00000441751.2:p.Arg21GlnfsTer8
ENST00000577817.3:c.219_220insT	ENSP00000467418.1:p.Gln74SerfsTer5
NM_000422.2:c.264_265insT	NP_000413.1:p.Gln89SerfsTer5
NM_000422.3:c.264_265insT MANE Select	NP_000413.1:p.Gln89SerfsTer5