Canonical Allele Identifier: CA2260105409
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624132C= , CM000679.2:g.41624132C= GRCh38
NC_000017.10:g.39780384C= , CM000679.1:g.39780384C= GRCh37
NC_000017.9:g.37033910C= NCBI36
NG_008625.1:g.5499G=
NG_009090.2:g.167581G= , LRG_401:g.167581G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.378G= MANE Select ENSP00000308452.8:p.Gly126=
ENST00000311208.12:c.378G= ENSP00000308452.8:p.Gly126=
ENST00000463128.5:c.-238G= ENSP00000468672.1:n.-238G=
ENST00000491673.1:n.444G=
ENST00000493253.5:n.165G=
ENST00000540235.5:c.129G= ENSP00000441751.2:p.Gly43=
ENST00000577817.3:c.333G= ENSP00000467418.1:p.Gly111=
NM_000422.2:c.378G= NP_000413.1:p.Gly126=
NM_000422.3:c.378G= MANE Select NP_000413.1:p.Gly126=