Canonical Allele Identifier: CA399512858
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780544A>C (hg19) chr17:g.41624292A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624292A>C , CM000679.2:g.41624292A>C GRCh38
NC_000017.10:g.39780544A>C , CM000679.1:g.39780544A>C GRCh37
NC_000017.9:g.37034070A>C NCBI36
NG_008625.1:g.5339T>G
NG_009090.2:g.167421T>G , LRG_401:g.167421T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.218T>G MANE Select ENSP00000308452.8:p.Phe73Cys
ENST00000311208.12:c.218T>G ENSP00000308452.8:p.Phe73Cys
ENST00000463128.5:c.-312-86T>G ENSP00000468672.1:n.-312-86T>G
ENST00000491673.1:n.284T>G
ENST00000493253.5:n.5T>G
ENST00000540235.5:c.13T>G ENSP00000441751.2:p.Leu5Val
ENST00000577817.3:c.173T>G ENSP00000467418.1:p.Phe58Cys
NM_000422.2:c.218T>G NP_000413.1:p.Phe73Cys
NM_000422.3:c.218T>G MANE Select NP_000413.1:p.Phe73Cys
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