Canonical Allele Identifier: CA500206342
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780471G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624219G>C , CM000679.2:g.41624219G>C GRCh38
NC_000017.10:g.39780471G>C , CM000679.1:g.39780471G>C GRCh37
NC_000017.9:g.37033997G>C NCBI36
NG_008625.1:g.5412C>G
NG_009090.2:g.167494C>G , LRG_401:g.167494C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.291C>G MANE Select ENSP00000308452.8:p.Ser97=
ENST00000311208.12:c.291C>G ENSP00000308452.8:p.Ser97=
ENST00000463128.5:c.-312-13C>G ENSP00000468672.1:n.-312-13C>G
ENST00000491673.1:n.357C>G
ENST00000493253.5:n.78C>G
ENST00000540235.5:c.71+15C>G ENSP00000441751.2:n.71+15C>G
ENST00000577817.3:c.246C>G ENSP00000467418.1:p.Ser82=
NM_000422.2:c.291C>G NP_000413.1:p.Ser97=
NM_000422.3:c.291C>G MANE Select NP_000413.1:p.Ser97=
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