Canonical Allele Identifier: CA216610
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14587
dbSNP Id: rs59151893

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624235T>C , CM000679.2:g.41624235T>C GRCh38
NC_000017.10:g.39780487T>C , CM000679.1:g.39780487T>C GRCh37
NC_000017.9:g.37034013T>C NCBI36
NG_008625.1:g.5396A>G
NG_009090.2:g.167478A>G , LRG_401:g.167478A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.275A>G MANE Select ENSP00000308452.8:p.Asn92Ser
ENST00000311208.12:c.275A>G ENSP00000308452.8:p.Asn92Ser
ENST00000463128.5:c.-312-29A>G ENSP00000468672.1:n.-312-29A>G
ENST00000491673.1:n.341A>G
ENST00000493253.5:n.62A>G
ENST00000540235.5:c.70A>G ENSP00000441751.2:p.Met24Val
ENST00000577817.3:c.230A>G ENSP00000467418.1:p.Asn77Ser
NM_000422.2:c.275A>G NP_000413.1:p.Asn92Ser
NM_000422.3:c.275A>G MANE Select NP_000413.1:p.Asn92Ser