Canonical Allele Identifier: CA2260105575

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624420C= , CM000679.2:g.41624420C=	GRCh38
NC_000017.10:g.39780672C= , CM000679.1:g.39780672C=	GRCh37
NC_000017.9:g.37034198C=	NCBI36
NG_008625.1:g.5211G=
NG_009090.2:g.167293G= , LRG_401:g.167293G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.90G= MANE Select	ENSP00000308452.8:p.Arg30=
ENST00000311208.12:c.90G=	ENSP00000308452.8:p.Arg30=
ENST00000463128.5:c.-312-214G=	ENSP00000468672.1:n.-312-214G=
ENST00000491673.1:n.156G=
ENST00000540235.5:c.-116G=	ENSP00000441751.2:n.-116G=
ENST00000577817.3:c.45G=	ENSP00000467418.1:p.Arg15=
NM_000422.2:c.90G=	NP_000413.1:p.Arg30=
NM_000422.3:c.90G= MANE Select	NP_000413.1:p.Arg30=