Canonical Allele Identifier: CA14081304
Gene: UNC13C HGNC NCBI

Linked Data

dbSNP Id: rs10518765

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.54388434A>C , CM000677.2:g.54388434A>C GRCh38
NC_000015.9:g.54680632A>C , CM000677.1:g.54680632A>C GRCh37
NC_000015.8:g.52467924A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260323.16:c.4714-4614A>C MANE Select ENSP00000260323.11:n.4714-4614A>C
ENST00000647821.1:c.4708-4614A>C ENSP00000497525.1:n.4708-4614A>C
ENST00000260323.15:c.4714-4614A>C ENSP00000260323.11:n.4714-4614A>C
ENST00000561210.1:n.1289-4614A>C
NM_001080534.1:c.4714-4614A>C NP_001074003.1:n.4714-4614A>C
XM_005254394.3:c.4714-4614A>C XP_005254451.1:n.4714-4614A>C
XM_005254395.3:c.4714-4614A>C XP_005254452.1:n.4714-4614A>C
NM_001080534.2:c.4714-4614A>C NP_001074003.1:n.4714-4614A>C
NM_001329919.1:c.4708-4614A>C NP_001316848.1:n.4708-4614A>C
XM_005254394.5:c.4714-4614A>C XP_005254451.1:n.4714-4614A>C
XM_017022220.1:c.4714-4614A>C XP_016877709.1:n.4714-4614A>C
XM_017022221.1:c.4714-4614A>C XP_016877710.1:n.4714-4614A>C
XM_017022222.1:c.4714-4614A>C XP_016877711.1:n.4714-4614A>C
XM_017022223.1:c.4708-4614A>C XP_016877712.1:n.4708-4614A>C
XM_017022225.1:c.1612-4614A>C XP_016877714.1:n.1612-4614A>C
XR_001751291.1:n.10897-4614A>C
NM_001329919.2:c.4708-4614A>C NP_001316848.1:n.4708-4614A>C
NM_001080534.3:c.4714-4614A>C MANE Select NP_001074003.1:n.4714-4614A>C