Canonical Allele Identifier: CA2260105456
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624214_41624229delinsAGGTAGGAGGCCAGGC , CM000679.2:g.41624214_41624229delinsAGGTAGGAGGCCAGGC GRCh38
NC_000017.10:g.39780466_39780481delinsAGGTAGGAGGCCAGGC , CM000679.1:g.39780466_39780481delinsAGGTAGGAGGCCAGGC GRCh37
NC_000017.9:g.37033992_37034007delinsAGGTAGGAGGCCAGGC NCBI36
NG_008625.1:g.5402_5417delinsGCCTGGCCTCCTACCT
NG_009090.2:g.167484_167499delinsGCCTGGCCTCCTACCT , LRG_401:g.167484_167499delinsGCCTGGCCTCCTACCT

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.281_296delinsGCCTGGCCTCCTACCT MANE Select ENSP00000308452.8:p.Arg94=
ENST00000311208.12:c.281_296delinsGCCTGGCCTCCTACCT ENSP00000308452.8:p.Arg94=
ENST00000463128.5:c.-312-23_-312-8delinsGCCTGGCCTCCTACCT ENSP00000468672.1:n.-312-23_-312-8delinsG...
ENST00000491673.1:n.347_362delinsGCCTGGCCTCCTACCT
ENST00000493253.5:n.68_83delinsGCCTGGCCTCCTACCT
ENST00000540235.5:c.71+5_71+20delinsGCCTGGCCTCCTACCT ENSP00000441751.2:n.71+5_71+20delinsGCCTG...
ENST00000577817.3:c.236_251delinsGCCTGGCCTCCTACCT ENSP00000467418.1:p.Arg79=
NM_000422.2:c.281_296delinsGCCTGGCCTCCTACCT NP_000413.1:p.Arg94=
NM_000422.3:c.281_296delinsGCCTGGCCTCCTACCT MANE Select NP_000413.1:p.Arg94=