Canonical Allele Identifier: CA216618
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs121912478

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624221_41624223del , CM000679.2:g.41624221_41624223del GRCh38
NC_000017.10:g.39780473_39780475del , CM000679.1:g.39780473_39780475del GRCh37
NC_000017.9:g.37033999_37034001del NCBI36
NG_008625.1:g.5411_5413del
NG_009090.2:g.167493_167495del , LRG_401:g.167493_167495del

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.290_292del MANE Select ENSP00000308452.8:p.Ser97del
ENST00000311208.12:c.290_292del ENSP00000308452.8:p.Ser97del
ENST00000463128.5:c.-312-14_-312-12del ENSP00000468672.1:n.-312-14_-312-12del
ENST00000491673.1:n.356_358del
ENST00000493253.5:n.77_79del
ENST00000540235.5:c.71+14_71+16del ENSP00000441751.2:n.71+14_71+16del
ENST00000577817.3:c.245_247del ENSP00000467418.1:p.Ser82del
NM_000422.2:c.290_292del NP_000413.1:p.Ser97del
NM_000422.3:c.290_292del MANE Select NP_000413.1:p.Ser97del