Canonical Allele Identifier: CA8563815
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs200102896

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624289C>A , CM000679.2:g.41624289C>A GRCh38
NC_000017.10:g.39780541C>A , CM000679.1:g.39780541C>A GRCh37
NC_000017.9:g.37034067C>A NCBI36
NG_008625.1:g.5342G>T
NG_009090.2:g.167424G>T , LRG_401:g.167424G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.221G>T MANE Select ENSP00000308452.8:p.Gly74Val
ENST00000311208.12:c.221G>T ENSP00000308452.8:p.Gly74Val
ENST00000463128.5:c.-312-83G>T ENSP00000468672.1:n.-312-83G>T
ENST00000491673.1:n.287G>T
ENST00000493253.5:n.8G>T
ENST00000540235.5:c.16G>T ENSP00000441751.2:p.Gly6Trp
ENST00000577817.3:c.176G>T ENSP00000467418.1:p.Gly59Val
NM_000422.2:c.221G>T NP_000413.1:p.Gly74Val
NM_000422.3:c.221G>T MANE Select NP_000413.1:p.Gly74Val