Canonical Allele Identifier: CA2260105489

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624270C= , CM000679.2:g.41624270C=	GRCh38
NC_000017.10:g.39780522C= , CM000679.1:g.39780522C=	GRCh37
NC_000017.9:g.37034048C=	NCBI36
NG_008625.1:g.5361G=
NG_009090.2:g.167443G= , LRG_401:g.167443G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.240G= MANE Select	ENSP00000308452.8:p.Leu80=
ENST00000311208.12:c.240G=	ENSP00000308452.8:p.Leu80=
ENST00000463128.5:c.-312-64G=	ENSP00000468672.1:n.-312-64G=
ENST00000491673.1:n.306G=
ENST00000493253.5:n.27G=
ENST00000540235.5:c.35G=	ENSP00000441751.2:p.Trp12=
ENST00000577817.3:c.195G=	ENSP00000467418.1:p.Leu65=
NM_000422.2:c.240G=	NP_000413.1:p.Leu80=
NM_000422.3:c.240G= MANE Select	NP_000413.1:p.Leu80=