Canonical Allele Identifier: CA2260105398

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624118T= , CM000679.2:g.41624118T=	GRCh38
NC_000017.10:g.39780370T= , CM000679.1:g.39780370T=	GRCh37
NC_000017.9:g.37033896T=	NCBI36
NG_008625.1:g.5513A=
NG_009090.2:g.167595A= , LRG_401:g.167595A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.392A= MANE Select	ENSP00000308452.8:p.Tyr131=
ENST00000311208.12:c.392A=	ENSP00000308452.8:p.Tyr131=
ENST00000463128.5:c.-224A=	ENSP00000468672.1:n.-224A=
ENST00000491673.1:n.458A=
ENST00000493253.5:n.179A=
ENST00000540235.5:c.143A=	ENSP00000441751.2:p.Tyr48=
ENST00000577817.3:c.347A=	ENSP00000467418.1:p.Tyr116=
NM_000422.2:c.392A=	NP_000413.1:p.Tyr131=
NM_000422.3:c.392A= MANE Select	NP_000413.1:p.Tyr131=