Canonical Allele Identifier: CA2637840891
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624218_41624219del , CM000679.2:g.41624218_41624219del GRCh38
NC_000017.10:g.39780470_39780471del , CM000679.1:g.39780470_39780471del GRCh37
NC_000017.9:g.37033996_37033997del NCBI36
NG_008625.1:g.5412_5413del
NG_009090.2:g.167494_167495del , LRG_401:g.167494_167495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.291_292del MANE Select ENSP00000308452.8:p.Tyr98ProfsTer13
ENST00000311208.12:c.291_292del ENSP00000308452.8:p.Tyr98ProfsTer13
ENST00000463128.5:c.-312-13_-312-12del ENSP00000468672.1:n.-312-13_-312-12del
ENST00000491673.1:n.357_358del
ENST00000493253.5:n.78_79del
ENST00000540235.5:c.71+15_71+16del ENSP00000441751.2:n.71+15_71+16del
ENST00000577817.3:c.246_247del ENSP00000467418.1:p.Tyr83ProfsTer13
NM_000422.2:c.291_292del NP_000413.1:p.Tyr98ProfsTer13
NM_000422.3:c.291_292del MANE Select NP_000413.1:p.Tyr98ProfsTer13