Canonical Allele Identifier: CA2637840888
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624109_41624126del , CM000679.2:g.41624109_41624126del GRCh38
NC_000017.10:g.39780361_39780378del , CM000679.1:g.39780361_39780378del GRCh37
NC_000017.9:g.37033887_37033904del NCBI36
NG_008625.1:g.5506_5523del
NG_009090.2:g.167588_167605del , LRG_401:g.167588_167605del

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.385_402del MANE Select ENSP00000308452.8:p.Arg129_Tyr134del
ENST00000311208.12:c.385_402del ENSP00000308452.8:p.Arg129_Tyr134del
ENST00000463128.5:c.-231_-214del ENSP00000468672.1:n.-231_-214del
ENST00000491673.1:n.451_468del
ENST00000493253.5:n.172_189del
ENST00000540235.5:c.136_153del ENSP00000441751.2:p.Arg46_Tyr51del
ENST00000577817.3:c.340_357del ENSP00000467418.1:p.Arg114_Tyr119del
NM_000422.2:c.385_402del NP_000413.1:p.Arg129_Tyr134del
NM_000422.3:c.385_402del MANE Select NP_000413.1:p.Arg129_Tyr134del