Canonical Allele Identifier: CA8563808
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs769139580

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624268G>A , CM000679.2:g.41624268G>A GRCh38
NC_000017.10:g.39780520G>A , CM000679.1:g.39780520G>A GRCh37
NC_000017.9:g.37034046G>A NCBI36
NG_008625.1:g.5363C>T
NG_009090.2:g.167445C>T , LRG_401:g.167445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.242C>T MANE Select ENSP00000308452.8:p.Ala81Val
ENST00000311208.12:c.242C>T ENSP00000308452.8:p.Ala81Val
ENST00000463128.5:c.-312-62C>T ENSP00000468672.1:n.-312-62C>T
ENST00000491673.1:n.308C>T
ENST00000493253.5:n.29C>T
ENST00000540235.5:c.37C>T ENSP00000441751.2:p.Leu13=
ENST00000577817.3:c.197C>T ENSP00000467418.1:p.Ala66Val
NM_000422.2:c.242C>T NP_000413.1:p.Ala81Val
NM_000422.3:c.242C>T MANE Select NP_000413.1:p.Ala81Val