Canonical Allele Identifier: CA2635613013

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002438_5002441del , CM000679.2:g.5002438_5002441del GRCh38
NC_000017.10:g.4905733_4905736del , CM000679.1:g.4905733_4905736del GRCh37
NC_000017.9:g.4846457_4846460del NCBI36
NG_034137.1:g.9491_9494del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.430-26_430-23del (KIF1C) MANE Select ENSP00000320821.5:n.430-26_430-23del
ENST00000320785.9:c.430-26_430-23del (KIF1C) ENSP00000320821.5:n.430-26_430-23del
NM_006612.5:c.430-26_430-23del (KIF1C) NP_006603.2:n.430-26_430-23del
XM_005256424.1:c.430-26_430-23del (KIF1C) XP_005256481.1:n.430-26_430-23del
XM_005256424.2:c.430-26_430-23del (KIF1C) XP_005256481.1:n.430-26_430-23del
XM_024450745.1:c.-39+3643_-39+3646del (INCA1) XP_024306513.1:n.-39+3643_-39+3646del
NM_006612.6:c.430-26_430-23del (KIF1C) MANE Select NP_006603.2:n.430-26_430-23del