Canonical Allele Identifier: CA399512211
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624178T>C , CM000679.2:g.41624178T>C GRCh38
NC_000017.10:g.39780430T>C , CM000679.1:g.39780430T>C GRCh37
NC_000017.9:g.37033956T>C NCBI36
NG_008625.1:g.5453A>G
NG_009090.2:g.167535A>G , LRG_401:g.167535A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.332A>G MANE Select ENSP00000308452.8:p.Glu111Gly
ENST00000311208.12:c.332A>G ENSP00000308452.8:p.Glu111Gly
ENST00000463128.5:c.-284A>G ENSP00000468672.1:n.-284A>G
ENST00000491673.1:n.398A>G
ENST00000493253.5:n.119A>G
ENST00000540235.5:c.83A>G ENSP00000441751.2:p.Glu28Gly
ENST00000577817.3:c.287A>G ENSP00000467418.1:p.Glu96Gly
NM_000422.2:c.332A>G NP_000413.1:p.Glu111Gly
NM_000422.3:c.332A>G MANE Select NP_000413.1:p.Glu111Gly