Canonical Allele Identifier: CA2260105480

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624254C= , CM000679.2:g.41624254C=	GRCh38
NC_000017.10:g.39780506C= , CM000679.1:g.39780506C=	GRCh37
NC_000017.9:g.37034032C=	NCBI36
NG_008625.1:g.5377G=
NG_009090.2:g.167459G= , LRG_401:g.167459G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.256G= MANE Select	ENSP00000308452.8:p.Ala86=
ENST00000311208.12:c.256G=	ENSP00000308452.8:p.Ala86=
ENST00000463128.5:c.-312-48G=	ENSP00000468672.1:n.-312-48G=
ENST00000491673.1:n.322G=
ENST00000493253.5:n.43G=
ENST00000540235.5:c.51G=	ENSP00000441751.2:p.Arg17=
ENST00000577817.3:c.211G=	ENSP00000467418.1:p.Ala71=
NM_000422.2:c.256G=	NP_000413.1:p.Ala86=
NM_000422.3:c.256G= MANE Select	NP_000413.1:p.Ala86=