Canonical Allele Identifier: CA399513964
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780739A>C (hg19) chr17:g.41624487A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624487A>C , CM000679.2:g.41624487A>C GRCh38
NC_000017.10:g.39780739A>C , CM000679.1:g.39780739A>C GRCh37
NC_000017.9:g.37034265A>C NCBI36
NG_008625.1:g.5144T>G
NG_009090.2:g.167226T>G , LRG_401:g.167226T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.23T>G MANE Select ENSP00000308452.8:p.Phe8Cys
ENST00000311208.12:c.23T>G ENSP00000308452.8:p.Phe8Cys
ENST00000463128.5:c.-313+256T>G ENSP00000468672.1:n.-313+256T>G
ENST00000491673.1:n.89T>G
ENST00000540235.5:c.-183T>G ENSP00000441751.2:n.-183T>G
NM_000422.2:c.23T>G NP_000413.1:p.Phe8Cys
NM_000422.3:c.23T>G MANE Select NP_000413.1:p.Phe8Cys
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