Canonical Allele Identifier: CA2260105678
Gene: KRT17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624560G= , CM000679.2:g.41624560G= GRCh38
NC_000017.10:g.39780812G= , CM000679.1:g.39780812G= GRCh37
NC_000017.9:g.37034338G= NCBI36
NG_008625.1:g.5071C=
NG_009090.2:g.167153C= , LRG_401:g.167153C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-51C= MANE Select ENSP00000308452.8:n.-51C=
ENST00000311208.12:c.-51C= ENSP00000308452.8:n.-51C=
ENST00000463128.5:c.-313+183C= ENSP00000468672.1:n.-313+183C=
ENST00000491673.1:n.16C=
NM_000422.2:c.-51C= NP_000413.1:n.-51C=
NM_000422.3:c.-51C= MANE Select NP_000413.1:n.-51C=
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