Canonical Allele Identifier: CA2635613161

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002552_5002553insA , CM000679.2:g.5002552_5002553insA GRCh38
NC_000017.10:g.4905847_4905848insA , CM000679.1:g.4905847_4905848insA GRCh37
NC_000017.9:g.4846571_4846572insA NCBI36
NG_034137.1:g.9605_9606insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.518_519insA (KIF1C) MANE Select ENSP00000320821.5:p.Leu174ProfsTer21
ENST00000320785.9:c.518_519insA (KIF1C) ENSP00000320821.5:p.Leu174ProfsTer21
NM_006612.5:c.518_519insA (KIF1C) NP_006603.2:p.Leu174ProfsTer21
XM_005256424.1:c.518_519insA (KIF1C) XP_005256481.1:p.Leu174ProfsTer21
XM_005256424.2:c.518_519insA (KIF1C) XP_005256481.1:p.Leu174ProfsTer21
XM_024450745.1:c.-39+3529_-39+3530insT (INCA1) XP_024306513.1:n.-39+3529_-39+3530insT
NM_006612.6:c.518_519insA (KIF1C) MANE Select NP_006603.2:p.Leu174ProfsTer21