Canonical Allele Identifier: CA2635613153

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002542del , CM000679.2:g.5002542del GRCh38
NC_000017.10:g.4905837del , CM000679.1:g.4905837del GRCh37
NC_000017.9:g.4846561del NCBI36
NG_034137.1:g.9595del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.508del (KIF1C) MANE Select ENSP00000320821.5:p.Glu170SerfsTer17
ENST00000320785.9:c.508del (KIF1C) ENSP00000320821.5:p.Glu170SerfsTer17
NM_006612.5:c.508del (KIF1C) NP_006603.2:p.Glu170SerfsTer17
XM_005256424.1:c.508del (KIF1C) XP_005256481.1:p.Glu170SerfsTer17
XM_005256424.2:c.508del (KIF1C) XP_005256481.1:p.Glu170SerfsTer17
XM_024450745.1:c.-39+3542del (INCA1) XP_024306513.1:n.-39+3542del
NM_006612.6:c.508del (KIF1C) MANE Select NP_006603.2:p.Glu170SerfsTer17