Canonical Allele Identifier: CA2260105404
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624128C= , CM000679.2:g.41624128C= GRCh38
NC_000017.10:g.39780380C= , CM000679.1:g.39780380C= GRCh37
NC_000017.9:g.37033906C= NCBI36
NG_008625.1:g.5503G=
NG_009090.2:g.167585G= , LRG_401:g.167585G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.382G= MANE Select ENSP00000308452.8:p.Ala128=
ENST00000311208.12:c.382G= ENSP00000308452.8:p.Ala128=
ENST00000463128.5:c.-234G= ENSP00000468672.1:n.-234G=
ENST00000491673.1:n.448G=
ENST00000493253.5:n.169G=
ENST00000540235.5:c.133G= ENSP00000441751.2:p.Ala45=
ENST00000577817.3:c.337G= ENSP00000467418.1:p.Ala113=
NM_000422.2:c.382G= NP_000413.1:p.Ala128=
NM_000422.3:c.382G= MANE Select NP_000413.1:p.Ala128=