Canonical Allele Identifier: CA2576268164

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624036_41624038del , CM000679.2:g.41624036_41624038del	GRCh38
NC_000017.10:g.39780288_39780290del , CM000679.1:g.39780288_39780290del	GRCh37
NC_000017.9:g.37033814_37033816del	NCBI36
NG_008625.1:g.5597_5599del
NG_009090.2:g.167679_167681del , LRG_401:g.167679_167681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+44_432+46del MANE Select	ENSP00000308452.8:n.432+44_432+46del
ENST00000311208.12:c.432+44_432+46del	ENSP00000308452.8:n.432+44_432+46del
ENST00000463128.5:c.-184+44_-184+46del	ENSP00000468672.1:n.-184+44_-184+46del
ENST00000491673.1:n.498+44_498+46del
ENST00000493253.5:n.219+44_219+46del
ENST00000540235.5:c.183+44_183+46del	ENSP00000441751.2:n.183+44_183+46del
ENST00000577817.3:c.387+44_387+46del	ENSP00000467418.1:n.387+44_387+46del
NM_000422.2:c.432+44_432+46del	NP_000413.1:n.432+44_432+46del
NM_000422.3:c.432+44_432+46del MANE Select	NP_000413.1:n.432+44_432+46del