Canonical Allele Identifier: CA2260105454
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624212_41624236delinsCCAGGTAGGAGGCCAGGCGGTCATT , CM000679.2:g.41624212_41624236delinsCCAGGTAGGAGGCCAGGCGGTCATT GRCh38
NC_000017.10:g.39780464_39780488delinsCCAGGTAGGAGGCCAGGCGGTCATT , CM000679.1:g.39780464_39780488delinsCCAGGTAGGAGGCCAGGCGGTCATT GRCh37
NC_000017.9:g.37033990_37034014delinsCCAGGTAGGAGGCCAGGCGGTCATT NCBI36
NG_008625.1:g.5395_5419delinsAATGACCGCCTGGCCTCCTACCTGG
NG_009090.2:g.167477_167501delinsAATGACCGCCTGGCCTCCTACCTGG , LRG_401:g.167477_167501delinsAATGACCGCCTGGCCTCCTACCTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.274_298delinsAATGACCGCCTGGCCTCCTACCTGG MANE Select ENSP00000308452.8:p.Asn92=
ENST00000311208.12:c.274_298delinsAATGACCGCCTGGCCTCCTACCTGG ENSP00000308452.8:p.Asn92=
ENST00000463128.5:c.-312-30_-312-6delinsAATGACCGCCTGGCCTCCTACCTGG ENSP00000468672.1:n.-312-30_-312-6delinsA...
ENST00000491673.1:n.340_364delinsAATGACCGCCTGGCCTCCTACCTGG
ENST00000493253.5:n.61_85delinsAATGACCGCCTGGCCTCCTACCTGG
ENST00000540235.5:c.69_72-21delinsAATGACCGCCTGGCCTCCTACCTGG
ENST00000577817.3:c.229_253delinsAATGACCGCCTGGCCTCCTACCTGG ENSP00000467418.1:p.Asn77=
NM_000422.2:c.274_298delinsAATGACCGCCTGGCCTCCTACCTGG NP_000413.1:p.Asn92=
NM_000422.3:c.274_298delinsAATGACCGCCTGGCCTCCTACCTGG MANE Select NP_000413.1:p.Asn92=