Canonical Allele Identifier: CA2260105660

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624536_41624539delinsCAGG , CM000679.2:g.41624536_41624539delinsCAGG	GRCh38
NC_000017.10:g.39780788_39780791delinsCAGG , CM000679.1:g.39780788_39780791delinsCAGG	GRCh37
NC_000017.9:g.37034314_37034317delinsCAGG	NCBI36
NG_008625.1:g.5092_5095delinsCCTG
NG_009090.2:g.167174_167177delinsCCTG , LRG_401:g.167174_167177delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-30_-27delinsCCTG MANE Select	ENSP00000308452.8:n.-30_-27delinsCCTG
ENST00000311208.12:c.-30_-27delinsCCTG	ENSP00000308452.8:n.-30_-27delinsCCTG
ENST00000463128.5:c.-313+204_-313+207delinsCCTG	ENSP00000468672.1:n.-313+204_-313+207delinsCCTG
ENST00000491673.1:n.37_40delinsCCTG
ENST00000540235.5:c.-235_-232delinsCCTG	ENSP00000441751.2:n.-235_-232delinsCCTG
NM_000422.2:c.-30_-27delinsCCTG	NP_000413.1:n.-30_-27delinsCCTG
NM_000422.3:c.-30_-27delinsCCTG MANE Select	NP_000413.1:n.-30_-27delinsCCTG