Canonical Allele Identifier: CA399511668
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624109T>C , CM000679.2:g.41624109T>C GRCh38
NC_000017.10:g.39780361T>C , CM000679.1:g.39780361T>C GRCh37
NC_000017.9:g.37033887T>C NCBI36
NG_008625.1:g.5522A>G
NG_009090.2:g.167604A>G , LRG_401:g.167604A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.401A>G MANE Select ENSP00000308452.8:p.Tyr134Cys
ENST00000311208.12:c.401A>G ENSP00000308452.8:p.Tyr134Cys
ENST00000463128.5:c.-215A>G ENSP00000468672.1:n.-215A>G
ENST00000491673.1:n.467A>G
ENST00000493253.5:n.188A>G
ENST00000540235.5:c.152A>G ENSP00000441751.2:p.Tyr51Cys
ENST00000577817.3:c.356A>G ENSP00000467418.1:p.Tyr119Cys
NM_000422.2:c.401A>G NP_000413.1:p.Tyr134Cys
NM_000422.3:c.401A>G MANE Select NP_000413.1:p.Tyr134Cys