Canonical Allele Identifier: CA2260105401
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624124C= , CM000679.2:g.41624124C= GRCh38
NC_000017.10:g.39780376C= , CM000679.1:g.39780376C= GRCh37
NC_000017.9:g.37033902C= NCBI36
NG_008625.1:g.5507G=
NG_009090.2:g.167589G= , LRG_401:g.167589G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.386G= MANE Select ENSP00000308452.8:p.Arg129=
ENST00000311208.12:c.386G= ENSP00000308452.8:p.Arg129=
ENST00000463128.5:c.-230G= ENSP00000468672.1:n.-230G=
ENST00000491673.1:n.452G=
ENST00000493253.5:n.173G=
ENST00000540235.5:c.137G= ENSP00000441751.2:p.Arg46=
ENST00000577817.3:c.341G= ENSP00000467418.1:p.Arg114=
NM_000422.2:c.386G= NP_000413.1:p.Arg129=
NM_000422.3:c.386G= MANE Select NP_000413.1:p.Arg129=