Canonical Allele Identifier: CA2260105505
Gene: KRT17 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.221G= MANE Select ENSP00000308452.8:p.Gly74=
ENST00000311208.12:c.221G= ENSP00000308452.8:p.Gly74=
ENST00000463128.5:c.-312-83G= ENSP00000468672.1:n.-312-83G=
ENST00000491673.1:n.287G=
ENST00000493253.5:n.8G=
ENST00000540235.5:c.16G= ENSP00000441751.2:p.Gly6=
ENST00000577817.3:c.176G= ENSP00000467418.1:p.Gly59=
NM_000422.2:c.221G= NP_000413.1:p.Gly74=
NM_000422.3:c.221G= MANE Select NP_000413.1:p.Gly74=