Canonical Allele Identifier: CA16611320
Gene: CACNA2D2 HGNC NCBI
CYB561D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 416549
ClinVar RCV Id: RCV000477086
dbSNP Id: rs1060504834
gnomAD v2: 3-50402405-G-A
gnomAD v4: 3-50364974-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50364974G>A , CM000665.2:g.50364974G>A GRCh38
NC_000003.11:g.50402405G>A , CM000665.1:g.50402405G>A GRCh37
NC_000003.10:g.50377409G>A NCBI36
NG_034070.1:g.144271C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000424201.7:c.3209-4C>T (CACNA2D2) MANE Select ENSP00000390329.2:n.3209-4C>T
ENST00000266039.7:c.3211C>T (CACNA2D2) ENSP00000266039.3:p.Pro1071Ser
ENST00000360963.7:c.3004C>T (CACNA2D2) ENSP00000354228.3:p.Pro1002Ser
ENST00000423994.6:c.3235C>T (CACNA2D2) ENSP00000407393.2:p.Pro1079Ser
ENST00000424201.6:c.3209-4C>T (CACNA2D2) ENSP00000390329.2:n.3209-4C>T
ENST00000429770.5:c.3212-4C>T (CACNA2D2) ENSP00000404631.1:n.3212-4C>T
ENST00000479441.1:c.3230-4C>T (CACNA2D2) ENSP00000418081.1:n.3230-4C>T
ENST00000483620.1:n.488C>T (CACNA2D2)
ENST00000606589.1:c.128-1323G>A ENSP00000476225.1:n.128-1323G>A
NM_001005505.2:c.3211C>T (CACNA2D2) NP_001005505.1:p.Pro1071Ser
NM_001174051.2:c.3230-4C>T (CACNA2D2) NP_001167522.1:n.3230-4C>T
NM_001291101.1:c.3004C>T (CACNA2D2) NP_001278030.1:p.Pro1002Ser
NM_006030.3:c.3209-4C>T (CACNA2D2) NP_006021.2:n.3209-4C>T
NR_111912.1:n.443-1323G>A (CYB561D2)
XM_005265581.3:c.3212-4C>T (CACNA2D2) XP_005265638.1:n.3212-4C>T
XM_011534242.1:c.3235C>T (CACNA2D2) XP_011532544.1:p.Pro1079Ser
XM_011534243.1:c.3233-4C>T (CACNA2D2) XP_011532545.1:n.3233-4C>T
XM_011534244.1:c.3214C>T (CACNA2D2) XP_011532546.1:p.Pro1072Ser
XM_005265581.4:c.3212-4C>T (CACNA2D2) XP_005265638.1:n.3212-4C>T
XM_011534243.2:c.3233-4C>T (CACNA2D2) XP_011532545.1:n.3233-4C>T
NM_001005505.3:c.3211C>T (CACNA2D2) NP_001005505.1:p.Pro1071Ser
NM_001174051.3:c.3230-4C>T (CACNA2D2) NP_001167522.1:n.3230-4C>T
NM_006030.4:c.3209-4C>T (CACNA2D2) MANE Select NP_006021.2:n.3209-4C>T
NR_111912.2:n.276-1323G>A (CYB561D2)