Canonical Allele Identifier: CA271159712

Gene: UNC13C

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.54576470G>A , CM000677.2:g.54576470G>A	GRCh38
NC_000015.9:g.54868668G>A , CM000677.1:g.54868668G>A	GRCh37
NC_000015.8:g.52655960G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260323.16:c.6106+8523G>A MANE Select	ENSP00000260323.11:n.6106+8523G>A
ENST00000647821.1:c.6100+8523G>A	ENSP00000497525.1:n.6100+8523G>A
ENST00000260323.15:c.6106+8523G>A	ENSP00000260323.11:n.6106+8523G>A
NM_001080534.1:c.6106+8523G>A	NP_001074003.1:n.6106+8523G>A
XM_005254394.3:c.6106+8523G>A	XP_005254451.1:n.6106+8523G>A
XM_005254395.3:c.6028+8523G>A	XP_005254452.1:n.6028+8523G>A
NM_001080534.2:c.6106+8523G>A	NP_001074003.1:n.6106+8523G>A
NM_001329919.1:c.6100+8523G>A	NP_001316848.1:n.6100+8523G>A
XM_005254394.5:c.6106+8523G>A	XP_005254451.1:n.6106+8523G>A
XM_017022220.1:c.6106+8523G>A	XP_016877709.1:n.6106+8523G>A
XM_017022221.1:c.6106+8523G>A	XP_016877710.1:n.6106+8523G>A
XM_017022222.1:c.6106+8523G>A	XP_016877711.1:n.6106+8523G>A
XM_017022223.1:c.6100+8523G>A	XP_016877712.1:n.6100+8523G>A
XM_017022225.1:c.3004+8523G>A	XP_016877714.1:n.3004+8523G>A
XR_001751291.1:n.12285+8523G>A
NM_001329919.2:c.6100+8523G>A	NP_001316848.1:n.6100+8523G>A
NM_001080534.3:c.6106+8523G>A MANE Select	NP_001074003.1:n.6106+8523G>A