Canonical Allele Identifier: CA397345972

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002542G>T , CM000679.2:g.5002542G>T GRCh38
NC_000017.10:g.4905837G>T , CM000679.1:g.4905837G>T GRCh37
NC_000017.9:g.4846561G>T NCBI36
NG_034137.1:g.9595G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.508G>T (KIF1C) MANE Select ENSP00000320821.5:p.Glu170Ter
ENST00000320785.9:c.508G>T (KIF1C) ENSP00000320821.5:p.Glu170Ter
NM_006612.5:c.508G>T (KIF1C) NP_006603.2:p.Glu170Ter
XM_005256424.1:c.508G>T (KIF1C) XP_005256481.1:p.Glu170Ter
XM_005256424.2:c.508G>T (KIF1C) XP_005256481.1:p.Glu170Ter
XM_024450745.1:c.-39+3540C>A (INCA1) XP_024306513.1:n.-39+3540C>A
NM_006612.6:c.508G>T (KIF1C) MANE Select NP_006603.2:p.Glu170Ter