Canonical Allele Identifier: CA2260105268

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623864_41623865delinsAG , CM000679.2:g.41623864_41623865delinsAG	GRCh38
NC_000017.10:g.39780116_39780117delinsAG , CM000679.1:g.39780116_39780117delinsAG	GRCh37
NC_000017.9:g.37033642_37033643delinsAG	NCBI36
NG_008625.1:g.5766_5767delinsCT
NG_009090.2:g.167848_167849delinsCT , LRG_401:g.167848_167849delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+213_432+214delinsCT MANE Select	ENSP00000308452.8:n.432+213_432+214delinsCT
ENST00000311208.12:c.432+213_432+214delinsCT	ENSP00000308452.8:n.432+213_432+214delinsCT
ENST00000463128.5:c.-184+213_-184+214delinsCT	ENSP00000468672.1:n.-184+213_-184+214delinsCT
ENST00000491673.1:n.498+213_498+214delinsCT
ENST00000493253.5:n.219+213_219+214delinsCT
ENST00000540235.5:c.183+213_183+214delinsCT	ENSP00000441751.2:n.183+213_183+214delinsCT
ENST00000577817.3:c.387+213_387+214delinsCT	ENSP00000467418.1:n.387+213_387+214delinsCT
NM_000422.2:c.432+213_432+214delinsCT	NP_000413.1:n.432+213_432+214delinsCT
NM_000422.3:c.432+213_432+214delinsCT MANE Select	NP_000413.1:n.432+213_432+214delinsCT