Canonical Allele Identifier: CA2260105519

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624322_41624331delinsAAGCTGTAGC , CM000679.2:g.41624322_41624331delinsAAGCTGTAGC	GRCh38
NC_000017.10:g.39780574_39780583delinsAAGCTGTAGC , CM000679.1:g.39780574_39780583delinsAAGCTGTAGC	GRCh37
NC_000017.9:g.37034100_37034109delinsAAGCTGTAGC	NCBI36
NG_008625.1:g.5300_5309delinsGCTACAGCTT
NG_009090.2:g.167382_167391delinsGCTACAGCTT , LRG_401:g.167382_167391delinsGCTACAGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.179_188delinsGCTACAGCTT MANE Select	ENSP00000308452.8:p.Cys60=
ENST00000311208.12:c.179_188delinsGCTACAGCTT	ENSP00000308452.8:p.Cys60=
ENST00000463128.5:c.-312-125_-312-116delinsGCTACAGCTT	ENSP00000468672.1:n.-312-125_-312-116delinsGCTACAGCTT
ENST00000491673.1:n.245_254delinsGCTACAGCTT
ENST00000540235.5:c.-27_-18delinsGCTACAGCTT	ENSP00000441751.2:n.-27_-18delinsGCTACAGCTT
ENST00000577817.3:c.134_143delinsGCTACAGCTT	ENSP00000467418.1:p.Cys45=
NM_000422.2:c.179_188delinsGCTACAGCTT	NP_000413.1:p.Cys60=
NM_000422.3:c.179_188delinsGCTACAGCTT MANE Select	NP_000413.1:p.Cys60=