Canonical Allele Identifier: CA399512946
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624304T>C , CM000679.2:g.41624304T>C GRCh38
NC_000017.10:g.39780556T>C , CM000679.1:g.39780556T>C GRCh37
NC_000017.9:g.37034082T>C NCBI36
NG_008625.1:g.5327A>G
NG_009090.2:g.167409A>G , LRG_401:g.167409A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.206A>G MANE Select ENSP00000308452.8:p.Tyr69Cys
ENST00000311208.12:c.206A>G ENSP00000308452.8:p.Tyr69Cys
ENST00000463128.5:c.-312-98A>G ENSP00000468672.1:n.-312-98A>G
ENST00000491673.1:n.272A>G
ENST00000540235.5:c.1A>G ENSP00000441751.2:p.Met1Val
ENST00000577817.3:c.161A>G ENSP00000467418.1:p.Tyr54Cys
NM_000422.2:c.206A>G NP_000413.1:p.Tyr69Cys
NM_000422.3:c.206A>G MANE Select NP_000413.1:p.Tyr69Cys