Canonical Allele Identifier: CA399512252
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624187G>C , CM000679.2:g.41624187G>C GRCh38
NC_000017.10:g.39780439G>C , CM000679.1:g.39780439G>C GRCh37
NC_000017.9:g.37033965G>C NCBI36
NG_008625.1:g.5444C>G
NG_009090.2:g.167526C>G , LRG_401:g.167526C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.323C>G MANE Select ENSP00000308452.8:p.Ala108Gly
ENST00000311208.12:c.323C>G ENSP00000308452.8:p.Ala108Gly
ENST00000463128.5:c.-293C>G ENSP00000468672.1:n.-293C>G
ENST00000491673.1:n.389C>G
ENST00000493253.5:n.110C>G
ENST00000540235.5:c.74C>G ENSP00000441751.2:p.Ala25Gly
ENST00000577817.3:c.278C>G ENSP00000467418.1:p.Ala93Gly
NM_000422.2:c.323C>G NP_000413.1:p.Ala108Gly
NM_000422.3:c.323C>G MANE Select NP_000413.1:p.Ala108Gly