Canonical Allele Identifier: CA2260105396

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624112T= , CM000679.2:g.41624112T=	GRCh38
NC_000017.10:g.39780364T= , CM000679.1:g.39780364T=	GRCh37
NC_000017.9:g.37033890T=	NCBI36
NG_008625.1:g.5519A=
NG_009090.2:g.167601A= , LRG_401:g.167601A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.398A= MANE Select	ENSP00000308452.8:p.Gln133=
ENST00000311208.12:c.398A=	ENSP00000308452.8:p.Gln133=
ENST00000463128.5:c.-218A=	ENSP00000468672.1:n.-218A=
ENST00000491673.1:n.464A=
ENST00000493253.5:n.185A=
ENST00000540235.5:c.149A=	ENSP00000441751.2:p.Gln50=
ENST00000577817.3:c.353A=	ENSP00000467418.1:p.Gln118=
NM_000422.2:c.398A=	NP_000413.1:p.Gln133=
NM_000422.3:c.398A= MANE Select	NP_000413.1:p.Gln133=