Canonical Allele Identifier: CA399513930
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780730G>T (hg19) chr17:g.41624478G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624478G>T , CM000679.2:g.41624478G>T GRCh38
NC_000017.10:g.39780730G>T , CM000679.1:g.39780730G>T GRCh37
NC_000017.9:g.37034256G>T NCBI36
NG_008625.1:g.5153C>A
NG_009090.2:g.167235C>A , LRG_401:g.167235C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.32C>A MANE Select ENSP00000308452.8:p.Ser11Tyr
ENST00000311208.12:c.32C>A ENSP00000308452.8:p.Ser11Tyr
ENST00000463128.5:c.-313+265C>A ENSP00000468672.1:n.-313+265C>A
ENST00000491673.1:n.98C>A
ENST00000540235.5:c.-174C>A ENSP00000441751.2:n.-174C>A
NM_000422.2:c.32C>A NP_000413.1:p.Ser11Tyr
NM_000422.3:c.32C>A MANE Select NP_000413.1:p.Ser11Tyr
Search 100 bp 5'
Search 100 bp 3'