Canonical Allele Identifier: CA2843181842

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002476dup , CM000679.2:g.5002476dup GRCh38
NC_000017.10:g.4905771dup , CM000679.1:g.4905771dup GRCh37
NC_000017.9:g.4846495dup NCBI36
NG_034137.1:g.9529dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.442dup (KIF1C) MANE Select ENSP00000320821.5:p.Glu148GlyfsTer5
ENST00000320785.9:c.442dup (KIF1C) ENSP00000320821.5:p.Glu148GlyfsTer5
NM_006612.5:c.442dup (KIF1C) NP_006603.2:p.Glu148GlyfsTer5
XM_005256424.1:c.442dup (KIF1C) XP_005256481.1:p.Glu148GlyfsTer5
XM_005256424.2:c.442dup (KIF1C) XP_005256481.1:p.Glu148GlyfsTer5
XM_024450745.1:c.-39+3607dup (INCA1) XP_024306513.1:n.-39+3607dup
NM_006612.6:c.442dup (KIF1C) MANE Select NP_006603.2:p.Glu148GlyfsTer5