Canonical Allele Identifier: CA8563787
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs781408687

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624139G>A , CM000679.2:g.41624139G>A GRCh38
NC_000017.10:g.39780391G>A , CM000679.1:g.39780391G>A GRCh37
NC_000017.9:g.37033917G>A NCBI36
NG_008625.1:g.5492C>T
NG_009090.2:g.167574C>T , LRG_401:g.167574C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.371C>T MANE Select ENSP00000308452.8:p.Ala124Val
ENST00000311208.12:c.371C>T ENSP00000308452.8:p.Ala124Val
ENST00000463128.5:c.-245C>T ENSP00000468672.1:n.-245C>T
ENST00000491673.1:n.437C>T
ENST00000493253.5:n.158C>T
ENST00000540235.5:c.122C>T ENSP00000441751.2:p.Ala41Val
ENST00000577817.3:c.326C>T ENSP00000467418.1:p.Ala109Val
NM_000422.2:c.371C>T NP_000413.1:p.Ala124Val
NM_000422.3:c.371C>T MANE Select NP_000413.1:p.Ala124Val