Canonical Allele Identifier: CA2565814169
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624038G>C , CM000679.2:g.41624038G>C GRCh38
NC_000017.10:g.39780290G>C , CM000679.1:g.39780290G>C GRCh37
NC_000017.9:g.37033816G>C NCBI36
NG_008625.1:g.5593C>G
NG_009090.2:g.167675C>G , LRG_401:g.167675C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+40C>G MANE Select ENSP00000308452.8:n.432+40C>G
ENST00000311208.12:c.432+40C>G ENSP00000308452.8:n.432+40C>G
ENST00000463128.5:c.-184+40C>G ENSP00000468672.1:n.-184+40C>G
ENST00000491673.1:n.498+40C>G
ENST00000493253.5:n.219+40C>G
ENST00000540235.5:c.183+40C>G ENSP00000441751.2:n.183+40C>G
ENST00000577817.3:c.387+40C>G ENSP00000467418.1:n.387+40C>G
NM_000422.2:c.432+40C>G NP_000413.1:n.432+40C>G
NM_000422.3:c.432+40C>G MANE Select NP_000413.1:n.432+40C>G