Canonical Allele Identifier: CA2260105610

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624468G= , CM000679.2:g.41624468G=	GRCh38
NC_000017.10:g.39780720G= , CM000679.1:g.39780720G=	GRCh37
NC_000017.9:g.37034246G=	NCBI36
NG_008625.1:g.5163C=
NG_009090.2:g.167245C= , LRG_401:g.167245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.42C= MANE Select	ENSP00000308452.8:p.Ile14=
ENST00000311208.12:c.42C=	ENSP00000308452.8:p.Ile14=
ENST00000463128.5:c.-312-262C=	ENSP00000468672.1:n.-312-262C=
ENST00000491673.1:n.108C=
ENST00000540235.5:c.-164C=	ENSP00000441751.2:n.-164C=
NM_000422.2:c.42C=	NP_000413.1:p.Ile14=
NM_000422.3:c.42C= MANE Select	NP_000413.1:p.Ile14=