Canonical Allele Identifier: CA2178293687

Gene: UNC13C

Genomic Alleles

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

Transcript Alleles

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