Canonical Allele Identifier: CA2260105646
Gene: KRT17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624519G= , CM000679.2:g.41624519G= GRCh38
NC_000017.10:g.39780771G= , CM000679.1:g.39780771G= GRCh37
NC_000017.9:g.37034297G= NCBI36
NG_008625.1:g.5112C=
NG_009090.2:g.167194C= , LRG_401:g.167194C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-10C= MANE Select ENSP00000308452.8:n.-10C=
ENST00000311208.12:c.-10C= ENSP00000308452.8:n.-10C=
ENST00000463128.5:c.-313+224C= ENSP00000468672.1:n.-313+224C=
ENST00000491673.1:n.57C=
ENST00000540235.5:c.-215C= ENSP00000441751.2:n.-215C=
NM_000422.2:c.-10C= NP_000413.1:n.-10C=
NM_000422.3:c.-10C= MANE Select NP_000413.1:n.-10C=
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