Canonical Allele Identifier: CA399512923
Gene: KRT17 HGNC NCBI

Linked Data

COSMIC: COSM979270

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624301C>T , CM000679.2:g.41624301C>T GRCh38
NC_000017.10:g.39780553C>T , CM000679.1:g.39780553C>T GRCh37
NC_000017.9:g.37034079C>T NCBI36
NG_008625.1:g.5330G>A
NG_009090.2:g.167412G>A , LRG_401:g.167412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.209G>A MANE Select ENSP00000308452.8:p.Gly70Asp
ENST00000311208.12:c.209G>A ENSP00000308452.8:p.Gly70Asp
ENST00000463128.5:c.-312-95G>A ENSP00000468672.1:n.-312-95G>A
ENST00000491673.1:n.275G>A
ENST00000540235.5:c.4G>A ENSP00000441751.2:p.Ala2Thr
ENST00000577817.3:c.164G>A ENSP00000467418.1:p.Gly55Asp
NM_000422.2:c.209G>A NP_000413.1:p.Gly70Asp
NM_000422.3:c.209G>A MANE Select NP_000413.1:p.Gly70Asp