Canonical Allele Identifier: CA399512160
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1597692917
MyVariant Identifiers: chr17:g.39780421A>C (hg19) chr17:g.41624169A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624169A>C , CM000679.2:g.41624169A>C GRCh38
NC_000017.10:g.39780421A>C , CM000679.1:g.39780421A>C GRCh37
NC_000017.9:g.37033947A>C NCBI36
NG_008625.1:g.5462T>G
NG_009090.2:g.167544T>G , LRG_401:g.167544T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.341T>G MANE Select ENSP00000308452.8:p.Val114Gly
ENST00000311208.12:c.341T>G ENSP00000308452.8:p.Val114Gly
ENST00000463128.5:c.-275T>G ENSP00000468672.1:n.-275T>G
ENST00000491673.1:n.407T>G
ENST00000493253.5:n.128T>G
ENST00000540235.5:c.92T>G ENSP00000441751.2:p.Val31Gly
ENST00000577817.3:c.296T>G ENSP00000467418.1:p.Val99Gly
NM_000422.2:c.341T>G NP_000413.1:p.Val114Gly
NM_000422.3:c.341T>G MANE Select NP_000413.1:p.Val114Gly
Search 100 bp 5'
Search 100 bp 3'