Canonical Allele Identifier: CA352900479

Gene: CACNA2D2 CYB561D2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50364932G>A , CM000665.2:g.50364932G>A	GRCh38
NC_000003.11:g.50402363G>A , CM000665.1:g.50402363G>A	GRCh37
NC_000003.10:g.50377367G>A	NCBI36
NG_034070.1:g.144313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424201.7:c.3247C>T (CACNA2D2) MANE Select	ENSP00000390329.2:p.Arg1083Ter
ENST00000266039.7:c.3253C>T (CACNA2D2)	ENSP00000266039.3:p.Arg1085Ter
ENST00000360963.7:c.3046C>T (CACNA2D2)	ENSP00000354228.3:p.Arg1016Ter
ENST00000423994.6:c.3277C>T (CACNA2D2)	ENSP00000407393.2:p.Arg1093Ter
ENST00000424201.6:c.3247C>T (CACNA2D2)	ENSP00000390329.2:p.Arg1083Ter
ENST00000429770.5:c.3250C>T (CACNA2D2)	ENSP00000404631.1:p.Arg1084Ter
ENST00000479441.1:c.3268C>T (CACNA2D2)	ENSP00000418081.1:p.Arg1090Ter
ENST00000483620.1:n.530C>T (CACNA2D2)
ENST00000606589.1:c.128-1365G>A	ENSP00000476225.1:n.128-1365G>A
NM_001005505.2:c.3253C>T (CACNA2D2)	NP_001005505.1:p.Arg1085Ter
NM_001174051.2:c.3268C>T (CACNA2D2)	NP_001167522.1:p.Arg1090Ter
NM_001291101.1:c.3046C>T (CACNA2D2)	NP_001278030.1:p.Arg1016Ter
NM_006030.3:c.3247C>T (CACNA2D2)	NP_006021.2:p.Arg1083Ter
NR_111912.1:n.443-1365G>A (CYB561D2)
XM_005265581.3:c.3250C>T (CACNA2D2)	XP_005265638.1:p.Arg1084Ter
XM_011534242.1:c.3277C>T (CACNA2D2)	XP_011532544.1:p.Arg1093Ter
XM_011534243.1:c.3271C>T (CACNA2D2)	XP_011532545.1:p.Arg1091Ter
XM_011534244.1:c.3256C>T (CACNA2D2)	XP_011532546.1:p.Arg1086Ter
XM_005265581.4:c.3250C>T (CACNA2D2)	XP_005265638.1:p.Arg1084Ter
XM_011534243.2:c.3271C>T (CACNA2D2)	XP_011532545.1:p.Arg1091Ter
NM_001005505.3:c.3253C>T (CACNA2D2)	NP_001005505.1:p.Arg1085Ter
NM_001174051.3:c.3268C>T (CACNA2D2)	NP_001167522.1:p.Arg1090Ter
NM_006030.4:c.3247C>T (CACNA2D2) MANE Select	NP_006021.2:p.Arg1083Ter
NR_111912.2:n.276-1365G>A (CYB561D2)