Canonical Allele Identifier: CA399512454
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624226A>C , CM000679.2:g.41624226A>C GRCh38
NC_000017.10:g.39780478A>C , CM000679.1:g.39780478A>C GRCh37
NC_000017.9:g.37034004A>C NCBI36
NG_008625.1:g.5405T>G
NG_009090.2:g.167487T>G , LRG_401:g.167487T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.284T>G MANE Select ENSP00000308452.8:p.Leu95Arg
ENST00000311208.12:c.284T>G ENSP00000308452.8:p.Leu95Arg
ENST00000463128.5:c.-312-20T>G ENSP00000468672.1:n.-312-20T>G
ENST00000491673.1:n.350T>G
ENST00000493253.5:n.71T>G
ENST00000540235.5:c.71+8T>G ENSP00000441751.2:n.71+8T>G
ENST00000577817.3:c.239T>G ENSP00000467418.1:p.Leu80Arg
NM_000422.2:c.284T>G NP_000413.1:p.Leu95Arg
NM_000422.3:c.284T>G MANE Select NP_000413.1:p.Leu95Arg