Canonical Allele Identifier: CA397345812

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002485T>G , CM000679.2:g.5002485T>G GRCh38
NC_000017.10:g.4905780T>G , CM000679.1:g.4905780T>G GRCh37
NC_000017.9:g.4846504T>G NCBI36
NG_034137.1:g.9538T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.451T>G (KIF1C) MANE Select ENSP00000320821.5:p.Cys151Gly
ENST00000320785.9:c.451T>G (KIF1C) ENSP00000320821.5:p.Cys151Gly
NM_006612.5:c.451T>G (KIF1C) NP_006603.2:p.Cys151Gly
XM_005256424.1:c.451T>G (KIF1C) XP_005256481.1:p.Cys151Gly
XM_005256424.2:c.451T>G (KIF1C) XP_005256481.1:p.Cys151Gly
XM_024450745.1:c.-39+3597A>C (INCA1) XP_024306513.1:n.-39+3597A>C
NM_006612.6:c.451T>G (KIF1C) MANE Select NP_006603.2:p.Cys151Gly