Canonical Allele Identifier: CA399512546
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1469282035

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624242T>G , CM000679.2:g.41624242T>G GRCh38
NC_000017.10:g.39780494T>G , CM000679.1:g.39780494T>G GRCh37
NC_000017.9:g.37034020T>G NCBI36
NG_008625.1:g.5389A>C
NG_009090.2:g.167471A>C , LRG_401:g.167471A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.268A>C MANE Select ENSP00000308452.8:p.Asn90His
ENST00000311208.12:c.268A>C ENSP00000308452.8:p.Asn90His
ENST00000463128.5:c.-312-36A>C ENSP00000468672.1:n.-312-36A>C
ENST00000491673.1:n.334A>C
ENST00000493253.5:n.55A>C
ENST00000540235.5:c.63A>C ENSP00000441751.2:p.Arg21Ser
ENST00000577817.3:c.223A>C ENSP00000467418.1:p.Asn75His
NM_000422.2:c.268A>C NP_000413.1:p.Asn90His
NM_000422.3:c.268A>C MANE Select NP_000413.1:p.Asn90His