Canonical Allele Identifier: CA2635613184

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002592_5002609del , CM000679.2:g.5002592_5002609del GRCh38
NC_000017.10:g.4905887_4905904del , CM000679.1:g.4905887_4905904del GRCh37
NC_000017.9:g.4846611_4846628del NCBI36
NG_034137.1:g.9645_9662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.558_575del (KIF1C) MANE Select ENSP00000320821.5:p.Thr187_Ile192del
ENST00000320785.9:c.558_575del (KIF1C) ENSP00000320821.5:p.Thr187_Ile192del
NM_006612.5:c.558_575del (KIF1C) NP_006603.2:p.Thr187_Ile192del
XM_005256424.1:c.558_575del (KIF1C) XP_005256481.1:p.Thr187_Ile192del
XM_005256424.2:c.558_575del (KIF1C) XP_005256481.1:p.Thr187_Ile192del
XM_024450745.1:c.-39+3474_-39+3491del (INCA1) XP_024306513.1:n.-39+3474_-39+3491del
NM_006612.6:c.558_575del (KIF1C) MANE Select NP_006603.2:p.Thr187_Ile192del