Canonical Allele Identifier: CA399513719
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780686G>C (hg19) chr17:g.41624434G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624434G>C , CM000679.2:g.41624434G>C GRCh38
NC_000017.10:g.39780686G>C , CM000679.1:g.39780686G>C GRCh37
NC_000017.9:g.37034212G>C NCBI36
NG_008625.1:g.5197C>G
NG_009090.2:g.167279C>G , LRG_401:g.167279C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.76C>G MANE Select ENSP00000308452.8:p.Arg26Gly
ENST00000311208.12:c.76C>G ENSP00000308452.8:p.Arg26Gly
ENST00000463128.5:c.-312-228C>G ENSP00000468672.1:n.-312-228C>G
ENST00000491673.1:n.142C>G
ENST00000540235.5:c.-130C>G ENSP00000441751.2:n.-130C>G
ENST00000577817.3:c.31C>G ENSP00000467418.1:p.Arg11Gly
NM_000422.2:c.76C>G NP_000413.1:p.Arg26Gly
NM_000422.3:c.76C>G MANE Select NP_000413.1:p.Arg26Gly
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Search 100 bp 3'