Canonical Allele Identifier: CA2260105639

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624513_41624515delinsGGC , CM000679.2:g.41624513_41624515delinsGGC	GRCh38
NC_000017.10:g.39780765_39780767delinsGGC , CM000679.1:g.39780765_39780767delinsGGC	GRCh37
NC_000017.9:g.37034291_37034293delinsGGC	NCBI36
NG_008625.1:g.5116_5118delinsGCC
NG_009090.2:g.167198_167200delinsGCC , LRG_401:g.167198_167200delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-6_-4delinsGCC MANE Select	ENSP00000308452.8:n.-6_-4delinsGCC
ENST00000311208.12:c.-6_-4delinsGCC	ENSP00000308452.8:n.-6_-4delinsGCC
ENST00000463128.5:c.-313+228_-313+230delinsGCC	ENSP00000468672.1:n.-313+228_-313+230delinsGCC
ENST00000491673.1:n.61_63delinsGCC
ENST00000540235.5:c.-211_-209delinsGCC	ENSP00000441751.2:n.-211_-209delinsGCC
NM_000422.2:c.-6_-4delinsGCC	NP_000413.1:n.-6_-4delinsGCC
NM_000422.3:c.-6_-4delinsGCC MANE Select	NP_000413.1:n.-6_-4delinsGCC