Canonical Allele Identifier: CA626215511
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1472134970

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624033A>G , CM000679.2:g.41624033A>G GRCh38
NC_000017.10:g.39780285A>G , CM000679.1:g.39780285A>G GRCh37
NC_000017.9:g.37033811A>G NCBI36
NG_008625.1:g.5598T>C
NG_009090.2:g.167680T>C , LRG_401:g.167680T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+45T>C MANE Select ENSP00000308452.8:n.432+45T>C
ENST00000311208.12:c.432+45T>C ENSP00000308452.8:n.432+45T>C
ENST00000463128.5:c.-184+45T>C ENSP00000468672.1:n.-184+45T>C
ENST00000491673.1:n.498+45T>C
ENST00000493253.5:n.219+45T>C
ENST00000540235.5:c.183+45T>C ENSP00000441751.2:n.183+45T>C
ENST00000577817.3:c.387+45T>C ENSP00000467418.1:n.387+45T>C
NM_000422.2:c.432+45T>C NP_000413.1:n.432+45T>C
NM_000422.3:c.432+45T>C MANE Select NP_000413.1:n.432+45T>C