Canonical Allele Identifier: CA399513676
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624424C>T , CM000679.2:g.41624424C>T GRCh38
NC_000017.10:g.39780676C>T , CM000679.1:g.39780676C>T GRCh37
NC_000017.9:g.37034202C>T NCBI36
NG_008625.1:g.5207G>A
NG_009090.2:g.167289G>A , LRG_401:g.167289G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.86G>A MANE Select ENSP00000308452.8:p.Cys29Tyr
ENST00000311208.12:c.86G>A ENSP00000308452.8:p.Cys29Tyr
ENST00000463128.5:c.-312-218G>A ENSP00000468672.1:n.-312-218G>A
ENST00000491673.1:n.152G>A
ENST00000540235.5:c.-120G>A ENSP00000441751.2:n.-120G>A
ENST00000577817.3:c.41G>A ENSP00000467418.1:p.Cys14Tyr
NM_000422.2:c.86G>A NP_000413.1:p.Cys29Tyr
NM_000422.3:c.86G>A MANE Select NP_000413.1:p.Cys29Tyr