Canonical Allele Identifier: CA2637840902
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624431_41624527del , CM000679.2:g.41624431_41624527del GRCh38
NC_000017.10:g.39780683_39780779del , CM000679.1:g.39780683_39780779del GRCh37
NC_000017.9:g.37034209_37034305del NCBI36
NG_008625.1:g.5114_5210del
NG_009090.2:g.167196_167292del , LRG_401:g.167196_167292del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-8_89del
ENST00000311208.12:c.-8_89del
ENST00000463128.5:c.-313+226_-312-215del ENSP00000468672.1:n.-313+226_-312-215del
ENST00000491673.1:n.59_155del
ENST00000540235.5:c.-213_-117del ENSP00000441751.2:n.-213_-117del
NM_000422.2:c.-8_89del
NM_000422.3:c.-8_89del