Canonical Allele Identifier: CA2244674673

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002621T= , CM000679.2:g.5002621T= GRCh38
NC_000017.10:g.4905916T= , CM000679.1:g.4905916T= GRCh37
NC_000017.9:g.4846640T= NCBI36
NG_034137.1:g.9674T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.587T= (KIF1C) MANE Select ENSP00000320821.5:p.Met196=
ENST00000320785.9:c.587T= (KIF1C) ENSP00000320821.5:p.Met196=
NM_006612.5:c.587T= (KIF1C) NP_006603.2:p.Met196=
XM_005256424.1:c.587T= (KIF1C) XP_005256481.1:p.Met196=
XM_005256424.2:c.587T= (KIF1C) XP_005256481.1:p.Met196=
XM_024450745.1:c.-39+3461A= (INCA1) XP_024306513.1:n.-39+3461A=
NM_006612.6:c.587T= (KIF1C) MANE Select NP_006603.2:p.Met196=