Canonical Allele Identifier: CA399511762
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624121T>G , CM000679.2:g.41624121T>G GRCh38
NC_000017.10:g.39780373T>G , CM000679.1:g.39780373T>G GRCh37
NC_000017.9:g.37033899T>G NCBI36
NG_008625.1:g.5510A>C
NG_009090.2:g.167592A>C , LRG_401:g.167592A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.389A>C MANE Select ENSP00000308452.8:p.Asp130Ala
ENST00000311208.12:c.389A>C ENSP00000308452.8:p.Asp130Ala
ENST00000463128.5:c.-227A>C ENSP00000468672.1:n.-227A>C
ENST00000491673.1:n.455A>C
ENST00000493253.5:n.176A>C
ENST00000540235.5:c.140A>C ENSP00000441751.2:p.Asp47Ala
ENST00000577817.3:c.344A>C ENSP00000467418.1:p.Asp115Ala
NM_000422.2:c.389A>C NP_000413.1:p.Asp130Ala
NM_000422.3:c.389A>C MANE Select NP_000413.1:p.Asp130Ala