Canonical Allele Identifier: CA352936551
Community Standard Title: NM_006030.4(CACNA2D2):c.1039C>T (p.Gln347Ter)
Gene: CACNA2D2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50379545G>A , CM000665.2:g.50379545G>A GRCh38
NC_000003.11:g.50416976G>A , CM000665.1:g.50416976G>A GRCh37
NC_000003.10:g.50391980G>A NCBI36
NG_034070.1:g.129700C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006030.4:c.1039C>T MANE Select NP_006021.2:p.Gln347Ter
ENST00000424201.7:c.1039C>T MANE Select ENSP00000390329.2:p.Gln347Ter
NM_001005505.2:c.1039C>T NP_001005505.1:p.Gln347Ter
NM_001005505.3:c.1039C>T NP_001005505.1:p.Gln347Ter
NM_001174051.2:c.1039C>T NP_001167522.1:p.Gln347Ter
NM_001174051.3:c.1039C>T NP_001167522.1:p.Gln347Ter
NM_001291101.1:c.832C>T NP_001278030.1:p.Gln278Ter
NM_006030.3:c.1039C>T NP_006021.2:p.Gln347Ter
ENST00000266039.7:c.1039C>T ENSP00000266039.3:p.Gln347Ter
ENST00000360963.7:c.832C>T ENSP00000354228.3:p.Gln278Ter
ENST00000423994.6:c.1039C>T ENSP00000407393.2:p.Gln347Ter
ENST00000424201.6:c.1039C>T ENSP00000390329.2:p.Gln347Ter
ENST00000429770.5:c.1039C>T ENSP00000404631.1:p.Gln347Ter
ENST00000479441.1:c.1039C>T ENSP00000418081.1:p.Gln347Ter
XM_005265581.3:c.1039C>T XP_005265638.1:p.Gln347Ter
XM_005265581.4:c.1039C>T XP_005265638.1:p.Gln347Ter
XM_011534242.1:c.1039C>T XP_011532544.1:p.Gln347Ter
XM_011534243.1:c.1039C>T XP_011532545.1:p.Gln347Ter
XM_011534243.2:c.1039C>T XP_011532545.1:p.Gln347Ter
XM_011534244.1:c.1039C>T XP_011532546.1:p.Gln347Ter