Canonical Allele Identifier: CA2260105391

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624097A= , CM000679.2:g.41624097A=	GRCh38
NC_000017.10:g.39780349A= , CM000679.1:g.39780349A=	GRCh37
NC_000017.9:g.37033875A=	NCBI36
NG_008625.1:g.5534T=
NG_009090.2:g.167616T= , LRG_401:g.167616T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.413T= MANE Select	ENSP00000308452.8:p.Ile138=
ENST00000311208.12:c.413T=	ENSP00000308452.8:p.Ile138=
ENST00000463128.5:c.-203T=	ENSP00000468672.1:n.-203T=
ENST00000491673.1:n.479T=
ENST00000493253.5:n.200T=
ENST00000540235.5:c.164T=	ENSP00000441751.2:p.Ile55=
ENST00000577817.3:c.368T=	ENSP00000467418.1:p.Ile123=
NM_000422.2:c.413T=	NP_000413.1:p.Ile138=
NM_000422.3:c.413T= MANE Select	NP_000413.1:p.Ile138=