Canonical Allele Identifier: CA2260105238
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1908628489
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41623807C>T , CM000679.2:g.41623807C>T GRCh38
NC_000017.10:g.39780059C>T , CM000679.1:g.39780059C>T GRCh37
NC_000017.9:g.37033585C>T NCBI36
NG_008625.1:g.5824G>A
NG_009090.2:g.167906G>A , LRG_401:g.167906G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+271G>A MANE Select ENSP00000308452.8:n.432+271G>A
ENST00000311208.12:c.432+271G>A ENSP00000308452.8:n.432+271G>A
ENST00000463128.5:c.-184+271G>A ENSP00000468672.1:n.-184+271G>A
ENST00000491673.1:n.498+271G>A
ENST00000493253.5:n.219+271G>A
ENST00000540235.5:c.183+271G>A ENSP00000441751.2:n.183+271G>A
ENST00000577817.3:c.387+271G>A ENSP00000467418.1:n.387+271G>A
NM_000422.2:c.432+271G>A NP_000413.1:n.432+271G>A
NM_000422.3:c.432+271G>A MANE Select NP_000413.1:n.432+271G>A
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