Canonical Allele Identifier: CA8563773
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs745933343

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624131dup , CM000679.2:g.41624131dup GRCh38
NC_000017.10:g.39780383dup , CM000679.1:g.39780383dup GRCh37
NC_000017.9:g.37033909dup NCBI36
NG_008625.1:g.5502dup
NG_009090.2:g.167584dup , LRG_401:g.167584dup

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.381dup MANE Select ENSP00000308452.8:p.Ala128ArgfsTer3
ENST00000311208.12:c.381dup ENSP00000308452.8:p.Ala128ArgfsTer3
ENST00000463128.5:c.-235dup ENSP00000468672.1:n.-235dup
ENST00000491673.1:n.447dup
ENST00000493253.5:n.168dup
ENST00000540235.5:c.132dup ENSP00000441751.2:p.Ala45ArgfsTer3
ENST00000577817.3:c.336dup ENSP00000467418.1:p.Ala113ArgfsTer3
NM_000422.2:c.381dup NP_000413.1:p.Ala128ArgfsTer3
NM_000422.3:c.381dup MANE Select NP_000413.1:p.Ala128ArgfsTer3