Canonical Allele Identifier: CA367892574
Gene: CACNA2D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81974473T>G , CM000669.2:g.81974473T>G GRCh38
NC_000007.13:g.81603789T>G , CM000669.1:g.81603789T>G GRCh37
NC_000007.12:g.81441725T>G NCBI36
NG_009358.2:g.474243A>C , LRG_437:g.474243A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000443883.2:c.2071A>C ENSP00000409374.2:p.Thr691Pro
ENST00000705961.1:c.1802A>C
ENST00000705962.1:c.1915A>C ENSP00000516190.1:p.Thr639Pro
ENST00000356860.8:c.2035A>C MANE Select ENSP00000349320.3:p.Thr679Pro
ENST00000356253.9:c.2071A>C ENSP00000348589.5:p.Thr691Pro
ENST00000356860.7:c.2035A>C ENSP00000349320.3:p.Thr679Pro
ENST00000443883.1:c.567A>C
NM_000722.3:c.2035A>C NP_000713.2:p.Thr679Pro
XM_005250570.1:c.2071A>C XP_005250627.1:p.Thr691Pro
XM_005250572.1:c.2020A>C XP_005250629.1:p.Thr674Pro
XM_005250573.1:c.2014A>C XP_005250630.1:p.Thr672Pro
XM_005250574.1:c.1999A>C XP_005250631.1:p.Thr667Pro
XM_006716118.1:c.2092A>C XP_006716181.1:p.Thr698Pro
XM_006716119.2:c.2017A>C XP_006716182.1:p.Thr673Pro
XM_006716120.2:c.1975A>C XP_006716183.1:p.Thr659Pro
XM_006716121.2:c.502A>C XP_006716184.1:p.Thr168Pro
XM_011516570.1:c.2092A>C XP_011514872.1:p.Thr698Pro
XM_011516571.1:c.2077A>C XP_011514873.1:p.Thr693Pro
XM_011516572.1:c.2056A>C XP_011514874.1:p.Thr686Pro
XM_011516573.1:c.1861A>C XP_011514875.1:p.Thr621Pro
NM_001366867.1:c.2071A>C NP_001353796.1:p.Thr691Pro
XM_005250572.3:c.2020A>C XP_005250629.1:p.Thr674Pro
XM_005250573.3:c.2014A>C XP_005250630.1:p.Thr672Pro
XM_005250574.3:c.1999A>C XP_005250631.1:p.Thr667Pro
XM_006716118.3:c.2092A>C XP_006716181.1:p.Thr698Pro
XM_006716119.3:c.2017A>C XP_006716182.1:p.Thr673Pro
XM_006716120.3:c.1975A>C XP_006716183.1:p.Thr659Pro
XM_006716121.3:c.502A>C XP_006716184.1:p.Thr168Pro
XM_011516570.3:c.2092A>C XP_011514872.1:p.Thr698Pro
XM_011516571.3:c.2077A>C XP_011514873.1:p.Thr693Pro
XM_011516572.3:c.2056A>C XP_011514874.1:p.Thr686Pro
XM_017012588.1:c.1918A>C XP_016868077.1:p.Thr640Pro
XR_001744873.2:n.2112A>C
XR_001744874.2:n.2019A>C
NM_000722.4:c.2035A>C MANE Select NP_000713.2:p.Thr679Pro