Canonical Allele Identifier: CA8318450

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5000791G>C , CM000679.2:g.5000791G>C GRCh38
NC_000017.10:g.4904086G>C , CM000679.1:g.4904086G>C GRCh37
NC_000017.9:g.4844810G>C NCBI36
NG_034137.1:g.7844G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006612.6:c.126G>C (KIF1C) MANE Select NP_006603.2:p.Gln42His
ENST00000320785.10:c.126G>C (KIF1C) MANE Select ENSP00000320821.5:p.Gln42His
NM_006612.5:c.126G>C (KIF1C) NP_006603.2:p.Gln42His
ENST00000320785.9:c.126G>C (KIF1C) ENSP00000320821.5:p.Gln42His
ENST00000574165.1:c.126G>C (KIF1C) ENSP00000458697.1:p.Gln42His
XM_005256424.1:c.126G>C (KIF1C) XP_005256481.1:p.Gln42His
XM_005256424.2:c.126G>C (KIF1C) XP_005256481.1:p.Gln42His
XM_024450745.1:c.-39+5291C>G (INCA1) XP_024306513.1:n.-39+5291C>G