Canonical Allele Identifier: CA399513064
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780574A>G (hg19) chr17:g.41624322A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624322A>G , CM000679.2:g.41624322A>G GRCh38
NC_000017.10:g.39780574A>G , CM000679.1:g.39780574A>G GRCh37
NC_000017.9:g.37034100A>G NCBI36
NG_008625.1:g.5309T>C
NG_009090.2:g.167391T>C , LRG_401:g.167391T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.188T>C MANE Select ENSP00000308452.8:p.Phe63Ser
ENST00000311208.12:c.188T>C ENSP00000308452.8:p.Phe63Ser
ENST00000463128.5:c.-312-116T>C ENSP00000468672.1:n.-312-116T>C
ENST00000491673.1:n.254T>C
ENST00000540235.5:c.-18T>C ENSP00000441751.2:n.-18T>C
ENST00000577817.3:c.143T>C ENSP00000467418.1:p.Phe48Ser
NM_000422.2:c.188T>C NP_000413.1:p.Phe63Ser
NM_000422.3:c.188T>C MANE Select NP_000413.1:p.Phe63Ser
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