Canonical Allele Identifier: CA2260105390

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624096A= , CM000679.2:g.41624096A=	GRCh38
NC_000017.10:g.39780348A= , CM000679.1:g.39780348A=	GRCh37
NC_000017.9:g.37033874A=	NCBI36
NG_008625.1:g.5535T=
NG_009090.2:g.167617T= , LRG_401:g.167617T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.414T= MANE Select	ENSP00000308452.8:p.Ile138=
ENST00000311208.12:c.414T=	ENSP00000308452.8:p.Ile138=
ENST00000463128.5:c.-202T=	ENSP00000468672.1:n.-202T=
ENST00000491673.1:n.480T=
ENST00000493253.5:n.201T=
ENST00000540235.5:c.165T=	ENSP00000441751.2:p.Ile55=
ENST00000577817.3:c.369T=	ENSP00000467418.1:p.Ile123=
NM_000422.2:c.414T=	NP_000413.1:p.Ile138=
NM_000422.3:c.414T= MANE Select	NP_000413.1:p.Ile138=