Canonical Allele Identifier: CA2260105585

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624434G= , CM000679.2:g.41624434G=	GRCh38
NC_000017.10:g.39780686G= , CM000679.1:g.39780686G=	GRCh37
NC_000017.9:g.37034212G=	NCBI36
NG_008625.1:g.5197C=
NG_009090.2:g.167279C= , LRG_401:g.167279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.76C= MANE Select	ENSP00000308452.8:p.Arg26=
ENST00000311208.12:c.76C=	ENSP00000308452.8:p.Arg26=
ENST00000463128.5:c.-312-228C=	ENSP00000468672.1:n.-312-228C=
ENST00000491673.1:n.142C=
ENST00000540235.5:c.-130C=	ENSP00000441751.2:n.-130C=
ENST00000577817.3:c.31C=	ENSP00000467418.1:p.Arg11=
NM_000422.2:c.76C=	NP_000413.1:p.Arg26=
NM_000422.3:c.76C= MANE Select	NP_000413.1:p.Arg26=