Canonical Allele Identifier: CA399512861
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624292A>G , CM000679.2:g.41624292A>G GRCh38
NC_000017.10:g.39780544A>G , CM000679.1:g.39780544A>G GRCh37
NC_000017.9:g.37034070A>G NCBI36
NG_008625.1:g.5339T>C
NG_009090.2:g.167421T>C , LRG_401:g.167421T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.218T>C MANE Select ENSP00000308452.8:p.Phe73Ser
ENST00000311208.12:c.218T>C ENSP00000308452.8:p.Phe73Ser
ENST00000463128.5:c.-312-86T>C ENSP00000468672.1:n.-312-86T>C
ENST00000491673.1:n.284T>C
ENST00000493253.5:n.5T>C
ENST00000540235.5:c.13T>C ENSP00000441751.2:p.Leu5=
ENST00000577817.3:c.173T>C ENSP00000467418.1:p.Phe58Ser
NM_000422.2:c.218T>C NP_000413.1:p.Phe73Ser
NM_000422.3:c.218T>C MANE Select NP_000413.1:p.Phe73Ser