Canonical Allele Identifier: CA2260105410
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624132_41624139delinsCCCCGGGG , CM000679.2:g.41624132_41624139delinsCCCCGGGG GRCh38
NC_000017.10:g.39780384_39780391delinsCCCCGGGG , CM000679.1:g.39780384_39780391delinsCCCCGGGG GRCh37
NC_000017.9:g.37033910_37033917delinsCCCCGGGG NCBI36
NG_008625.1:g.5492_5499delinsCCCCGGGG
NG_009090.2:g.167574_167581delinsCCCCGGGG , LRG_401:g.167574_167581delinsCCCCGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.371_378delinsCCCCGGGG MANE Select ENSP00000308452.8:p.Ala124=
ENST00000311208.12:c.371_378delinsCCCCGGGG ENSP00000308452.8:p.Ala124=
ENST00000463128.5:c.-245_-238delinsCCCCGGGG ENSP00000468672.1:n.-245_-238delinsCCCCGG...
ENST00000491673.1:n.437_444delinsCCCCGGGG
ENST00000493253.5:n.158_165delinsCCCCGGGG
ENST00000540235.5:c.122_129delinsCCCCGGGG ENSP00000441751.2:p.Ala41=
ENST00000577817.3:c.326_333delinsCCCCGGGG ENSP00000467418.1:p.Ala109=
NM_000422.2:c.371_378delinsCCCCGGGG NP_000413.1:p.Ala124=
NM_000422.3:c.371_378delinsCCCCGGGG MANE Select NP_000413.1:p.Ala124=