Canonical Allele Identifier: CA399513631
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780667G>C (hg19) chr17:g.41624415G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624415G>C , CM000679.2:g.41624415G>C GRCh38
NC_000017.10:g.39780667G>C , CM000679.1:g.39780667G>C GRCh37
NC_000017.9:g.37034193G>C NCBI36
NG_008625.1:g.5216C>G
NG_009090.2:g.167298C>G , LRG_401:g.167298C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.95C>G MANE Select ENSP00000308452.8:p.Ser32Cys
ENST00000311208.12:c.95C>G ENSP00000308452.8:p.Ser32Cys
ENST00000463128.5:c.-312-209C>G ENSP00000468672.1:n.-312-209C>G
ENST00000491673.1:n.161C>G
ENST00000540235.5:c.-111C>G ENSP00000441751.2:n.-111C>G
ENST00000577817.3:c.50C>G ENSP00000467418.1:p.Ser17Cys
NM_000422.2:c.95C>G NP_000413.1:p.Ser32Cys
NM_000422.3:c.95C>G MANE Select NP_000413.1:p.Ser32Cys
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