Canonical Allele Identifier: CA2178277187

Gene: UNC13C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.54371421C= , CM000677.2:g.54371421C=	GRCh38
NC_000015.9:g.54663619C= , CM000677.1:g.54663619C=	GRCh37
NC_000015.8:g.52450911C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080534.3:c.4714-21627C= MANE Select	NP_001074003.1:n.4714-21627C=
ENST00000260323.16:c.4714-21627C= MANE Select	ENSP00000260323.11:n.4714-21627C=
NM_001080534.1:c.4714-21627C=	NP_001074003.1:n.4714-21627C=
NM_001080534.2:c.4714-21627C=	NP_001074003.1:n.4714-21627C=
NM_001329919.1:c.4708-21627C=	NP_001316848.1:n.4708-21627C=
NM_001329919.2:c.4708-21627C=	NP_001316848.1:n.4708-21627C=
ENST00000260323.15:c.4714-21627C=	ENSP00000260323.11:n.4714-21627C=
ENST00000561210.1:n.1289-21627C=
ENST00000647821.1:c.4708-21627C=	ENSP00000497525.1:n.4708-21627C=
XM_005254394.3:c.4714-21627C=	XP_005254451.1:n.4714-21627C=
XM_005254394.5:c.4714-21627C=	XP_005254451.1:n.4714-21627C=
XM_005254395.3:c.4714-21627C=	XP_005254452.1:n.4714-21627C=
XM_017022220.1:c.4714-21627C=	XP_016877709.1:n.4714-21627C=
XM_017022221.1:c.4714-21627C=	XP_016877710.1:n.4714-21627C=
XM_017022222.1:c.4714-21627C=	XP_016877711.1:n.4714-21627C=
XM_017022223.1:c.4708-21627C=	XP_016877712.1:n.4708-21627C=
XM_017022225.1:c.1612-21627C=	XP_016877714.1:n.1612-21627C=
XR_001751291.1:n.10897-21627C=