Canonical Allele Identifier: CA2260105422

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624155A= , CM000679.2:g.41624155A=	GRCh38
NC_000017.10:g.39780407A= , CM000679.1:g.39780407A=	GRCh37
NC_000017.9:g.37033933A=	NCBI36
NG_008625.1:g.5476T=
NG_009090.2:g.167558T= , LRG_401:g.167558T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.355T= MANE Select	ENSP00000308452.8:p.Trp119=
ENST00000311208.12:c.355T=	ENSP00000308452.8:p.Trp119=
ENST00000463128.5:c.-261T=	ENSP00000468672.1:n.-261T=
ENST00000491673.1:n.421T=
ENST00000493253.5:n.142T=
ENST00000540235.5:c.106T=	ENSP00000441751.2:p.Trp36=
ENST00000577817.3:c.310T=	ENSP00000467418.1:p.Trp104=
NM_000422.2:c.355T=	NP_000413.1:p.Trp119=
NM_000422.3:c.355T= MANE Select	NP_000413.1:p.Trp119=