Canonical Allele Identifier: CA8318576

Linked Data

dbSNP Id: rs756493686
gnomAD v2: 17-4905778-A-G
gnomAD v3: 17-5002483-A-G
gnomAD v4: 17-5002483-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002483A>G , CM000679.2:g.5002483A>G GRCh38
NC_000017.10:g.4905778A>G , CM000679.1:g.4905778A>G GRCh37
NC_000017.9:g.4846502A>G NCBI36
NG_034137.1:g.9536A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.449A>G (KIF1C) MANE Select ENSP00000320821.5:p.Tyr150Cys
ENST00000320785.9:c.449A>G (KIF1C) ENSP00000320821.5:p.Tyr150Cys
NM_006612.5:c.449A>G (KIF1C) NP_006603.2:p.Tyr150Cys
XM_005256424.1:c.449A>G (KIF1C) XP_005256481.1:p.Tyr150Cys
XM_005256424.2:c.449A>G (KIF1C) XP_005256481.1:p.Tyr150Cys
XM_024450745.1:c.-39+3599T>C (INCA1) XP_024306513.1:n.-39+3599T>C
NM_006612.6:c.449A>G (KIF1C) MANE Select NP_006603.2:p.Tyr150Cys