Canonical Allele Identifier: CA2418100
Gene: CACNA2D2 HGNC NCBI
CYB561D2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50364768C>T , CM000665.2:g.50364768C>T GRCh38
NC_000003.11:g.50402199C>T , CM000665.1:g.50402199C>T GRCh37
NC_000003.10:g.50377203C>T NCBI36
NG_034070.1:g.144477G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424201.7:c.3330G>A (CACNA2D2) MANE Select ENSP00000390329.2:p.Pro1110=
ENST00000266039.7:c.3336G>A (CACNA2D2) ENSP00000266039.3:p.Pro1112=
ENST00000360963.7:c.3129G>A (CACNA2D2) ENSP00000354228.3:p.Pro1043=
ENST00000423994.6:c.3360G>A (CACNA2D2) ENSP00000407393.2:p.Pro1120=
ENST00000424201.6:c.3330G>A (CACNA2D2) ENSP00000390329.2:p.Pro1110=
ENST00000429770.5:c.3333G>A (CACNA2D2) ENSP00000404631.1:p.Pro1111=
ENST00000479441.1:c.3351G>A (CACNA2D2) ENSP00000418081.1:p.Pro1117=
ENST00000483620.1:n.613G>A (CACNA2D2)
ENST00000606589.1:c.128-1529C>T ENSP00000476225.1:n.128-1529C>T
NM_001005505.2:c.3336G>A (CACNA2D2) NP_001005505.1:p.Pro1112=
NM_001174051.2:c.3351G>A (CACNA2D2) NP_001167522.1:p.Pro1117=
NM_001291101.1:c.3129G>A (CACNA2D2) NP_001278030.1:p.Pro1043=
NM_006030.3:c.3330G>A (CACNA2D2) NP_006021.2:p.Pro1110=
NR_111912.1:n.443-1529C>T (CYB561D2)
XM_005265581.3:c.3333G>A (CACNA2D2) XP_005265638.1:p.Pro1111=
XM_011534242.1:c.3360G>A (CACNA2D2) XP_011532544.1:p.Pro1120=
XM_011534243.1:c.3354G>A (CACNA2D2) XP_011532545.1:p.Pro1118=
XM_011534244.1:c.3339G>A (CACNA2D2) XP_011532546.1:p.Pro1113=
XM_005265581.4:c.3333G>A (CACNA2D2) XP_005265638.1:p.Pro1111=
XM_011534243.2:c.3354G>A (CACNA2D2) XP_011532545.1:p.Pro1118=
NM_001005505.3:c.3336G>A (CACNA2D2) NP_001005505.1:p.Pro1112=
NM_001174051.3:c.3351G>A (CACNA2D2) NP_001167522.1:p.Pro1117=
NM_006030.4:c.3330G>A (CACNA2D2) MANE Select NP_006021.2:p.Pro1110=
NR_111912.2:n.276-1529C>T (CYB561D2)