Canonical Allele Identifier: CA2260105491

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624272_41624273delinsGC , CM000679.2:g.41624272_41624273delinsGC	GRCh38
NC_000017.10:g.39780524_39780525delinsGC , CM000679.1:g.39780524_39780525delinsGC	GRCh37
NC_000017.9:g.37034050_37034051delinsGC	NCBI36
NG_008625.1:g.5358_5359delinsGC
NG_009090.2:g.167440_167441delinsGC , LRG_401:g.167440_167441delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.237_238delinsGC MANE Select	ENSP00000308452.8:p.Leu79=
ENST00000311208.12:c.237_238delinsGC	ENSP00000308452.8:p.Leu79=
ENST00000463128.5:c.-312-67_-312-66delinsGC	ENSP00000468672.1:n.-312-67_-312-66delinsGC
ENST00000491673.1:n.303_304delinsGC
ENST00000493253.5:n.24_25delinsGC
ENST00000540235.5:c.32_33delinsGC	ENSP00000441751.2:p.Cys11=
ENST00000577817.3:c.192_193delinsGC	ENSP00000467418.1:p.Leu64=
NM_000422.2:c.237_238delinsGC	NP_000413.1:p.Leu79=
NM_000422.3:c.237_238delinsGC MANE Select	NP_000413.1:p.Leu79=