Canonical Allele Identifier: CA8318463

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5000865G>C , CM000679.2:g.5000865G>C GRCh38
NC_000017.10:g.4904160G>C , CM000679.1:g.4904160G>C GRCh37
NC_000017.9:g.4844884G>C NCBI36
NG_034137.1:g.7918G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006612.6:c.183+17G>C (KIF1C) MANE Select NP_006603.2:n.183+17G>C
ENST00000320785.10:c.183+17G>C (KIF1C) MANE Select ENSP00000320821.5:n.183+17G>C
NM_006612.5:c.183+17G>C (KIF1C) NP_006603.2:n.183+17G>C
ENST00000320785.9:c.183+17G>C (KIF1C) ENSP00000320821.5:n.183+17G>C
ENST00000574165.1:c.183+17G>C (KIF1C) ENSP00000458697.1:n.183+17G>C
XM_005256424.1:c.183+17G>C (KIF1C) XP_005256481.1:n.183+17G>C
XM_005256424.2:c.183+17G>C (KIF1C) XP_005256481.1:n.183+17G>C
XM_024450745.1:c.-39+5217C>G (INCA1) XP_024306513.1:n.-39+5217C>G