Canonical Allele Identifier: CA2244674532

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002536G= , CM000679.2:g.5002536G= GRCh38
NC_000017.10:g.4905831G= , CM000679.1:g.4905831G= GRCh37
NC_000017.9:g.4846555G= NCBI36
NG_034137.1:g.9589G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.502G= (KIF1C) MANE Select ENSP00000320821.5:p.Val168=
ENST00000320785.9:c.502G= (KIF1C) ENSP00000320821.5:p.Val168=
NM_006612.5:c.502G= (KIF1C) NP_006603.2:p.Val168=
XM_005256424.1:c.502G= (KIF1C) XP_005256481.1:p.Val168=
XM_005256424.2:c.502G= (KIF1C) XP_005256481.1:p.Val168=
XM_024450745.1:c.-39+3546C= (INCA1) XP_024306513.1:n.-39+3546C=
NM_006612.6:c.502G= (KIF1C) MANE Select NP_006603.2:p.Val168=