Canonical Allele Identifier: CA500206231
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780417C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624165C>T , CM000679.2:g.41624165C>T GRCh38
NC_000017.10:g.39780417C>T , CM000679.1:g.39780417C>T GRCh37
NC_000017.9:g.37033943C>T NCBI36
NG_008625.1:g.5466G>A
NG_009090.2:g.167548G>A , LRG_401:g.167548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.345G>A MANE Select ENSP00000308452.8:p.Lys115=
ENST00000311208.12:c.345G>A ENSP00000308452.8:p.Lys115=
ENST00000463128.5:c.-271G>A ENSP00000468672.1:n.-271G>A
ENST00000491673.1:n.411G>A
ENST00000493253.5:n.132G>A
ENST00000540235.5:c.96G>A ENSP00000441751.2:p.Lys32=
ENST00000577817.3:c.300G>A ENSP00000467418.1:p.Lys100=
NM_000422.2:c.345G>A NP_000413.1:p.Lys115=
NM_000422.3:c.345G>A MANE Select NP_000413.1:p.Lys115=
Search 100 bp 5'
Search 100 bp 3'