Canonical Allele Identifier: CA287209923

Linked Data

dbSNP Id: rs964164823

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4998708G>A , CM000679.2:g.4998708G>A GRCh38
NC_000017.10:g.4902003G>A , CM000679.1:g.4902003G>A GRCh37
NC_000017.9:g.4842727G>A NCBI36
NG_034137.1:g.5761G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320785.10:c.-149+552G>A (KIF1C) MANE Select ENSP00000320821.5:n.-149+552G>A
ENST00000320785.9:c.-149+552G>A (KIF1C) ENSP00000320821.5:n.-149+552G>A
ENST00000574165.1:c.-182-305G>A (KIF1C) ENSP00000458697.1:n.-182-305G>A
NM_006612.5:c.-149+552G>A (KIF1C) NP_006603.2:n.-149+552G>A
XM_005256424.1:c.-182-305G>A (KIF1C) XP_005256481.1:n.-182-305G>A
XM_005256424.2:c.-182-305G>A (KIF1C) XP_005256481.1:n.-182-305G>A
XM_024450745.1:c.-38-4233C>T (INCA1) XP_024306513.1:n.-38-4233C>T
NM_006612.6:c.-149+552G>A (KIF1C) MANE Select NP_006603.2:n.-149+552G>A