Canonical Allele Identifier: CA399512315
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624199G>A , CM000679.2:g.41624199G>A GRCh38
NC_000017.10:g.39780451G>A , CM000679.1:g.39780451G>A GRCh37
NC_000017.9:g.37033977G>A NCBI36
NG_008625.1:g.5432C>T
NG_009090.2:g.167514C>T , LRG_401:g.167514C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.311C>T MANE Select ENSP00000308452.8:p.Ala104Val
ENST00000311208.12:c.311C>T ENSP00000308452.8:p.Ala104Val
ENST00000463128.5:c.-305C>T ENSP00000468672.1:n.-305C>T
ENST00000491673.1:n.377C>T
ENST00000493253.5:n.98C>T
ENST00000540235.5:c.72-8C>T ENSP00000441751.2:n.72-8C>T
ENST00000577817.3:c.266C>T ENSP00000467418.1:p.Ala89Val
NM_000422.2:c.311C>T NP_000413.1:p.Ala104Val
NM_000422.3:c.311C>T MANE Select NP_000413.1:p.Ala104Val