Canonical Allele Identifier: CA367892904
Gene: CACNA2D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81974537G>C , CM000669.2:g.81974537G>C GRCh38
NC_000007.13:g.81603853G>C , CM000669.1:g.81603853G>C GRCh37
NC_000007.12:g.81441789G>C NCBI36
NG_009358.2:g.474179C>G , LRG_437:g.474179C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000443883.2:c.2007C>G ENSP00000409374.2:p.Asp669Glu
ENST00000705961.1:c.1738C>G
ENST00000705962.1:c.1851C>G ENSP00000516190.1:p.Asp617Glu
ENST00000356860.8:c.1971C>G MANE Select ENSP00000349320.3:p.Asp657Glu
ENST00000356253.9:c.2007C>G ENSP00000348589.5:p.Asp669Glu
ENST00000356860.7:c.1971C>G ENSP00000349320.3:p.Asp657Glu
ENST00000443883.1:c.503C>G
NM_000722.3:c.1971C>G NP_000713.2:p.Asp657Glu
XM_005250570.1:c.2007C>G XP_005250627.1:p.Asp669Glu
XM_005250572.1:c.1956C>G XP_005250629.1:p.Asp652Glu
XM_005250573.1:c.1950C>G XP_005250630.1:p.Asp650Glu
XM_005250574.1:c.1935C>G XP_005250631.1:p.Asp645Glu
XM_006716118.1:c.2028C>G XP_006716181.1:p.Asp676Glu
XM_006716119.2:c.1953C>G XP_006716182.1:p.Asp651Glu
XM_006716120.2:c.1911C>G XP_006716183.1:p.Asp637Glu
XM_006716121.2:c.438C>G XP_006716184.1:p.Asp146Glu
XM_011516570.1:c.2028C>G XP_011514872.1:p.Asp676Glu
XM_011516571.1:c.2013C>G XP_011514873.1:p.Asp671Glu
XM_011516572.1:c.1992C>G XP_011514874.1:p.Asp664Glu
XM_011516573.1:c.1797C>G XP_011514875.1:p.Asp599Glu
NM_001366867.1:c.2007C>G NP_001353796.1:p.Asp669Glu
XM_005250572.3:c.1956C>G XP_005250629.1:p.Asp652Glu
XM_005250573.3:c.1950C>G XP_005250630.1:p.Asp650Glu
XM_005250574.3:c.1935C>G XP_005250631.1:p.Asp645Glu
XM_006716118.3:c.2028C>G XP_006716181.1:p.Asp676Glu
XM_006716119.3:c.1953C>G XP_006716182.1:p.Asp651Glu
XM_006716120.3:c.1911C>G XP_006716183.1:p.Asp637Glu
XM_006716121.3:c.438C>G XP_006716184.1:p.Asp146Glu
XM_011516570.3:c.2028C>G XP_011514872.1:p.Asp676Glu
XM_011516571.3:c.2013C>G XP_011514873.1:p.Asp671Glu
XM_011516572.3:c.1992C>G XP_011514874.1:p.Asp664Glu
XM_017012588.1:c.1854C>G XP_016868077.1:p.Asp618Glu
XR_001744873.2:n.2048C>G
XR_001744874.2:n.1955C>G
NM_000722.4:c.1971C>G MANE Select NP_000713.2:p.Asp657Glu