Canonical Allele Identifier: CA397345964

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002537T>A , CM000679.2:g.5002537T>A GRCh38
NC_000017.10:g.4905832T>A , CM000679.1:g.4905832T>A GRCh37
NC_000017.9:g.4846556T>A NCBI36
NG_034137.1:g.9590T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.503T>A (KIF1C) MANE Select ENSP00000320821.5:p.Val168Asp
ENST00000320785.9:c.503T>A (KIF1C) ENSP00000320821.5:p.Val168Asp
NM_006612.5:c.503T>A (KIF1C) NP_006603.2:p.Val168Asp
XM_005256424.1:c.503T>A (KIF1C) XP_005256481.1:p.Val168Asp
XM_005256424.2:c.503T>A (KIF1C) XP_005256481.1:p.Val168Asp
XM_024450745.1:c.-39+3545A>T (INCA1) XP_024306513.1:n.-39+3545A>T
NM_006612.6:c.503T>A (KIF1C) MANE Select NP_006603.2:p.Val168Asp