Canonical Allele Identifier: CA2244668434

Linked Data

dbSNP Id: rs1337339740

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4998695C>G , CM000679.2:g.4998695C>G GRCh38
NC_000017.10:g.4901990C>G , CM000679.1:g.4901990C>G GRCh37
NC_000017.9:g.4842714C>G NCBI36
NG_034137.1:g.5748C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320785.10:c.-149+539C>G (KIF1C) MANE Select ENSP00000320821.5:n.-149+539C>G
ENST00000320785.9:c.-149+539C>G (KIF1C) ENSP00000320821.5:n.-149+539C>G
ENST00000574165.1:c.-182-318C>G (KIF1C) ENSP00000458697.1:n.-182-318C>G
NM_006612.5:c.-149+539C>G (KIF1C) NP_006603.2:n.-149+539C>G
XM_005256424.1:c.-182-318C>G (KIF1C) XP_005256481.1:n.-182-318C>G
XM_005256424.2:c.-182-318C>G (KIF1C) XP_005256481.1:n.-182-318C>G
XM_024450745.1:c.-38-4220G>C (INCA1) XP_024306513.1:n.-38-4220G>C
NM_006612.6:c.-149+539C>G (KIF1C) MANE Select NP_006603.2:n.-149+539C>G