Canonical Allele Identifier: CA399512155
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624167T>C , CM000679.2:g.41624167T>C GRCh38
NC_000017.10:g.39780419T>C , CM000679.1:g.39780419T>C GRCh37
NC_000017.9:g.37033945T>C NCBI36
NG_008625.1:g.5464A>G
NG_009090.2:g.167546A>G , LRG_401:g.167546A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.343A>G MANE Select ENSP00000308452.8:p.Lys115Glu
ENST00000311208.12:c.343A>G ENSP00000308452.8:p.Lys115Glu
ENST00000463128.5:c.-273A>G ENSP00000468672.1:n.-273A>G
ENST00000491673.1:n.409A>G
ENST00000493253.5:n.130A>G
ENST00000540235.5:c.94A>G ENSP00000441751.2:p.Lys32Glu
ENST00000577817.3:c.298A>G ENSP00000467418.1:p.Lys100Glu
NM_000422.2:c.343A>G NP_000413.1:p.Lys115Glu
NM_000422.3:c.343A>G MANE Select NP_000413.1:p.Lys115Glu