Canonical Allele Identifier: CA2260105229
Gene: KRT17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41623792T= , CM000679.2:g.41623792T= GRCh38
NC_000017.10:g.39780044T= , CM000679.1:g.39780044T= GRCh37
NC_000017.9:g.37033570T= NCBI36
NG_008625.1:g.5839A=
NG_009090.2:g.167921A= , LRG_401:g.167921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+286A= MANE Select ENSP00000308452.8:n.432+286A=
ENST00000311208.12:c.432+286A= ENSP00000308452.8:n.432+286A=
ENST00000463128.5:c.-184+286A= ENSP00000468672.1:n.-184+286A=
ENST00000491673.1:n.498+286A=
ENST00000493253.5:n.219+286A=
ENST00000540235.5:c.183+286A= ENSP00000441751.2:n.183+286A=
ENST00000577817.3:c.387+286A= ENSP00000467418.1:n.387+286A=
NM_000422.2:c.432+286A= NP_000413.1:n.432+286A=
NM_000422.3:c.432+286A= MANE Select NP_000413.1:n.432+286A=
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