Canonical Allele Identifier: CA2260105525

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624331C= , CM000679.2:g.41624331C=	GRCh38
NC_000017.10:g.39780583C= , CM000679.1:g.39780583C=	GRCh37
NC_000017.9:g.37034109C=	NCBI36
NG_008625.1:g.5300G=
NG_009090.2:g.167382G= , LRG_401:g.167382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.179G= MANE Select	ENSP00000308452.8:p.Cys60=
ENST00000311208.12:c.179G=	ENSP00000308452.8:p.Cys60=
ENST00000463128.5:c.-312-125G=	ENSP00000468672.1:n.-312-125G=
ENST00000491673.1:n.245G=
ENST00000540235.5:c.-27G=	ENSP00000441751.2:n.-27G=
ENST00000577817.3:c.134G=	ENSP00000467418.1:p.Cys45=
NM_000422.2:c.179G=	NP_000413.1:p.Cys60=
NM_000422.3:c.179G= MANE Select	NP_000413.1:p.Cys60=