Canonical Allele Identifier: CA2260105465
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624230G= , CM000679.2:g.41624230G= GRCh38
NC_000017.10:g.39780482G= , CM000679.1:g.39780482G= GRCh37
NC_000017.9:g.37034008G= NCBI36
NG_008625.1:g.5401C=
NG_009090.2:g.167483C= , LRG_401:g.167483C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.280C= MANE Select ENSP00000308452.8:p.Arg94=
ENST00000311208.12:c.280C= ENSP00000308452.8:p.Arg94=
ENST00000463128.5:c.-312-24C= ENSP00000468672.1:n.-312-24C=
ENST00000491673.1:n.346C=
ENST00000493253.5:n.67C=
ENST00000540235.5:c.71+4C= ENSP00000441751.2:n.71+4C=
ENST00000577817.3:c.235C= ENSP00000467418.1:p.Arg79=
NM_000422.2:c.280C= NP_000413.1:p.Arg94=
NM_000422.3:c.280C= MANE Select NP_000413.1:p.Arg94=