Canonical Allele Identifier: CA2260105532

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624348_41624349delinsAC , CM000679.2:g.41624348_41624349delinsAC	GRCh38
NC_000017.10:g.39780600_39780601delinsAC , CM000679.1:g.39780600_39780601delinsAC	GRCh37
NC_000017.9:g.37034126_37034127delinsAC	NCBI36
NG_008625.1:g.5282_5283delinsGT
NG_009090.2:g.167364_167365delinsGT , LRG_401:g.167364_167365delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.161_162delinsGT MANE Select	ENSP00000308452.8:p.Gly54=
ENST00000311208.12:c.161_162delinsGT	ENSP00000308452.8:p.Gly54=
ENST00000463128.5:c.-312-143_-312-142delinsGT	ENSP00000468672.1:n.-312-143_-312-142delinsGT
ENST00000491673.1:n.227_228delinsGT
ENST00000540235.5:c.-45_-44delinsGT	ENSP00000441751.2:n.-45_-44delinsGT
ENST00000577817.3:c.116_117delinsGT	ENSP00000467418.1:p.Gly39=
NM_000422.2:c.161_162delinsGT	NP_000413.1:p.Gly54=
NM_000422.3:c.161_162delinsGT MANE Select	NP_000413.1:p.Gly54=