Canonical Allele Identifier: CA2260105500

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624285_41624286delinsAC , CM000679.2:g.41624285_41624286delinsAC	GRCh38
NC_000017.10:g.39780537_39780538delinsAC , CM000679.1:g.39780537_39780538delinsAC	GRCh37
NC_000017.9:g.37034063_37034064delinsAC	NCBI36
NG_008625.1:g.5345_5346delinsGT
NG_009090.2:g.167427_167428delinsGT , LRG_401:g.167427_167428delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.224_225delinsGT MANE Select	ENSP00000308452.8:p.Gly75=
ENST00000311208.12:c.224_225delinsGT	ENSP00000308452.8:p.Gly75=
ENST00000463128.5:c.-312-80_-312-79delinsGT	ENSP00000468672.1:n.-312-80_-312-79delinsGT
ENST00000491673.1:n.290_291delinsGT
ENST00000493253.5:n.11_12delinsGT
ENST00000540235.5:c.19_20delinsGT	ENSP00000441751.2:p.Val7=
ENST00000577817.3:c.179_180delinsGT	ENSP00000467418.1:p.Gly60=
NM_000422.2:c.224_225delinsGT	NP_000413.1:p.Gly75=
NM_000422.3:c.224_225delinsGT MANE Select	NP_000413.1:p.Gly75=