Canonical Allele Identifier: CA2244674550

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002541G= , CM000679.2:g.5002541G= GRCh38
NC_000017.10:g.4905836G= , CM000679.1:g.4905836G= GRCh37
NC_000017.9:g.4846560G= NCBI36
NG_034137.1:g.9594G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.507G= (KIF1C) MANE Select ENSP00000320821.5:p.Arg169=
ENST00000320785.9:c.507G= (KIF1C) ENSP00000320821.5:p.Arg169=
NM_006612.5:c.507G= (KIF1C) NP_006603.2:p.Arg169=
XM_005256424.1:c.507G= (KIF1C) XP_005256481.1:p.Arg169=
XM_005256424.2:c.507G= (KIF1C) XP_005256481.1:p.Arg169=
XM_024450745.1:c.-39+3541C= (INCA1) XP_024306513.1:n.-39+3541C=
NM_006612.6:c.507G= (KIF1C) MANE Select NP_006603.2:p.Arg169=