Canonical Allele Identifier: CA399513132
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624331C>T , CM000679.2:g.41624331C>T GRCh38
NC_000017.10:g.39780583C>T , CM000679.1:g.39780583C>T GRCh37
NC_000017.9:g.37034109C>T NCBI36
NG_008625.1:g.5300G>A
NG_009090.2:g.167382G>A , LRG_401:g.167382G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.179G>A MANE Select ENSP00000308452.8:p.Cys60Tyr
ENST00000311208.12:c.179G>A ENSP00000308452.8:p.Cys60Tyr
ENST00000463128.5:c.-312-125G>A ENSP00000468672.1:n.-312-125G>A
ENST00000491673.1:n.245G>A
ENST00000540235.5:c.-27G>A ENSP00000441751.2:n.-27G>A
ENST00000577817.3:c.134G>A ENSP00000467418.1:p.Cys45Tyr
NM_000422.2:c.179G>A NP_000413.1:p.Cys60Tyr
NM_000422.3:c.179G>A MANE Select NP_000413.1:p.Cys60Tyr