Canonical Allele Identifier: CA2260105453
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624211_41624223delinsTCCAGGTAGGAGG , CM000679.2:g.41624211_41624223delinsTCCAGGTAGGAGG GRCh38
NC_000017.10:g.39780463_39780475delinsTCCAGGTAGGAGG , CM000679.1:g.39780463_39780475delinsTCCAGGTAGGAGG GRCh37
NC_000017.9:g.37033989_37034001delinsTCCAGGTAGGAGG NCBI36
NG_008625.1:g.5408_5420delinsCCTCCTACCTGGA
NG_009090.2:g.167490_167502delinsCCTCCTACCTGGA , LRG_401:g.167490_167502delinsCCTCCTACCTGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.287_299delinsCCTCCTACCTGGA MANE Select ENSP00000308452.8:p.Ala96=
ENST00000311208.12:c.287_299delinsCCTCCTACCTGGA ENSP00000308452.8:p.Ala96=
ENST00000463128.5:c.-312-17_-312-5delinsCCTCCTACCTGGA ENSP00000468672.1:n.-312-17_-312-5delinsC...
ENST00000491673.1:n.353_365delinsCCTCCTACCTGGA
ENST00000493253.5:n.74_86delinsCCTCCTACCTGGA
ENST00000540235.5:c.71+11_72-20delinsCCTCCTACCTGGA ENSP00000441751.2:n.71+11_72-20delinsCCTC...
ENST00000577817.3:c.242_254delinsCCTCCTACCTGGA ENSP00000467418.1:p.Ala81=
NM_000422.2:c.287_299delinsCCTCCTACCTGGA NP_000413.1:p.Ala96=
NM_000422.3:c.287_299delinsCCTCCTACCTGGA MANE Select NP_000413.1:p.Ala96=