Canonical Allele Identifier: CA2260105403
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624127G= , CM000679.2:g.41624127G= GRCh38
NC_000017.10:g.39780379G= , CM000679.1:g.39780379G= GRCh37
NC_000017.9:g.37033905G= NCBI36
NG_008625.1:g.5504C=
NG_009090.2:g.167586C= , LRG_401:g.167586C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.383C= MANE Select ENSP00000308452.8:p.Ala128=
ENST00000311208.12:c.383C= ENSP00000308452.8:p.Ala128=
ENST00000463128.5:c.-233C= ENSP00000468672.1:n.-233C=
ENST00000491673.1:n.449C=
ENST00000493253.5:n.170C=
ENST00000540235.5:c.134C= ENSP00000441751.2:p.Ala45=
ENST00000577817.3:c.338C= ENSP00000467418.1:p.Ala113=
NM_000422.2:c.383C= NP_000413.1:p.Ala128=
NM_000422.3:c.383C= MANE Select NP_000413.1:p.Ala128=