Canonical Allele Identifier: CA2260105622
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624494G= , CM000679.2:g.41624494G= GRCh38
NC_000017.10:g.39780746G= , CM000679.1:g.39780746G= GRCh37
NC_000017.9:g.37034272G= NCBI36
NG_008625.1:g.5137C=
NG_009090.2:g.167219C= , LRG_401:g.167219C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.16C= MANE Select ENSP00000308452.8:p.Arg6=
ENST00000311208.12:c.16C= ENSP00000308452.8:p.Arg6=
ENST00000463128.5:c.-313+249C= ENSP00000468672.1:n.-313+249C=
ENST00000491673.1:n.82C=
ENST00000540235.5:c.-190C= ENSP00000441751.2:n.-190C=
NM_000422.2:c.16C= NP_000413.1:p.Arg6=
NM_000422.3:c.16C= MANE Select NP_000413.1:p.Arg6=