Canonical Allele Identifier: CA2260105640

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624514_41624515delinsGC , CM000679.2:g.41624514_41624515delinsGC	GRCh38
NC_000017.10:g.39780766_39780767delinsGC , CM000679.1:g.39780766_39780767delinsGC	GRCh37
NC_000017.9:g.37034292_37034293delinsGC	NCBI36
NG_008625.1:g.5116_5117delinsGC
NG_009090.2:g.167198_167199delinsGC , LRG_401:g.167198_167199delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-6_-5delinsGC MANE Select	ENSP00000308452.8:n.-6_-5delinsGC
ENST00000311208.12:c.-6_-5delinsGC	ENSP00000308452.8:n.-6_-5delinsGC
ENST00000463128.5:c.-313+228_-313+229delinsGC	ENSP00000468672.1:n.-313+228_-313+229delinsGC
ENST00000491673.1:n.61_62delinsGC
ENST00000540235.5:c.-211_-210delinsGC	ENSP00000441751.2:n.-211_-210delinsGC
NM_000422.2:c.-6_-5delinsGC	NP_000413.1:n.-6_-5delinsGC
NM_000422.3:c.-6_-5delinsGC MANE Select	NP_000413.1:n.-6_-5delinsGC