Canonical Allele Identifier: CA399511565
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780349A>C (hg19) chr17:g.41624097A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624097A>C , CM000679.2:g.41624097A>C GRCh38
NC_000017.10:g.39780349A>C , CM000679.1:g.39780349A>C GRCh37
NC_000017.9:g.37033875A>C NCBI36
NG_008625.1:g.5534T>G
NG_009090.2:g.167616T>G , LRG_401:g.167616T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.413T>G MANE Select ENSP00000308452.8:p.Ile138Ser
ENST00000311208.12:c.413T>G ENSP00000308452.8:p.Ile138Ser
ENST00000463128.5:c.-203T>G ENSP00000468672.1:n.-203T>G
ENST00000491673.1:n.479T>G
ENST00000493253.5:n.200T>G
ENST00000540235.5:c.164T>G ENSP00000441751.2:p.Ile55Ser
ENST00000577817.3:c.368T>G ENSP00000467418.1:p.Ile123Ser
NM_000422.2:c.413T>G NP_000413.1:p.Ile138Ser
NM_000422.3:c.413T>G MANE Select NP_000413.1:p.Ile138Ser
Search 100 bp 5'
Search 100 bp 3'