Canonical Allele Identifier: CA2260105406
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624131G= , CM000679.2:g.41624131G= GRCh38
NC_000017.10:g.39780383G= , CM000679.1:g.39780383G= GRCh37
NC_000017.9:g.37033909G= NCBI36
NG_008625.1:g.5500C=
NG_009090.2:g.167582C= , LRG_401:g.167582C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.379C= MANE Select ENSP00000308452.8:p.Pro127=
ENST00000311208.12:c.379C= ENSP00000308452.8:p.Pro127=
ENST00000463128.5:c.-237C= ENSP00000468672.1:n.-237C=
ENST00000491673.1:n.445C=
ENST00000493253.5:n.166C=
ENST00000540235.5:c.130C= ENSP00000441751.2:p.Pro44=
ENST00000577817.3:c.334C= ENSP00000467418.1:p.Pro112=
NM_000422.2:c.379C= NP_000413.1:p.Pro127=
NM_000422.3:c.379C= MANE Select NP_000413.1:p.Pro127=