Canonical Allele Identifier: CA2260105361

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624043_41624044delinsGC , CM000679.2:g.41624043_41624044delinsGC	GRCh38
NC_000017.10:g.39780295_39780296delinsGC , CM000679.1:g.39780295_39780296delinsGC	GRCh37
NC_000017.9:g.37033821_37033822delinsGC	NCBI36
NG_008625.1:g.5587_5588delinsGC
NG_009090.2:g.167669_167670delinsGC , LRG_401:g.167669_167670delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+34_432+35delinsGC MANE Select	ENSP00000308452.8:n.432+34_432+35delinsGC
ENST00000311208.12:c.432+34_432+35delinsGC	ENSP00000308452.8:n.432+34_432+35delinsGC
ENST00000463128.5:c.-184+34_-184+35delinsGC	ENSP00000468672.1:n.-184+34_-184+35delinsGC
ENST00000491673.1:n.498+34_498+35delinsGC
ENST00000493253.5:n.219+34_219+35delinsGC
ENST00000540235.5:c.183+34_183+35delinsGC	ENSP00000441751.2:n.183+34_183+35delinsGC
ENST00000577817.3:c.387+34_387+35delinsGC	ENSP00000467418.1:n.387+34_387+35delinsGC
NM_000422.2:c.432+34_432+35delinsGC	NP_000413.1:n.432+34_432+35delinsGC
NM_000422.3:c.432+34_432+35delinsGC MANE Select	NP_000413.1:n.432+34_432+35delinsGC