Canonical Allele Identifier: CA2178399952

Gene: UNC13C

Genomic Alleles

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

Transcript Alleles

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