Canonical Allele Identifier: CA367892582
Gene: CACNA2D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81974476T>G , CM000669.2:g.81974476T>G GRCh38
NC_000007.13:g.81603792T>G , CM000669.1:g.81603792T>G GRCh37
NC_000007.12:g.81441728T>G NCBI36
NG_009358.2:g.474240A>C , LRG_437:g.474240A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000443883.2:c.2068A>C ENSP00000409374.2:p.Lys690Gln
ENST00000705961.1:c.1799A>C
ENST00000705962.1:c.1912A>C ENSP00000516190.1:p.Lys638Gln
ENST00000356860.8:c.2032A>C MANE Select ENSP00000349320.3:p.Lys678Gln
ENST00000356253.9:c.2068A>C ENSP00000348589.5:p.Lys690Gln
ENST00000356860.7:c.2032A>C ENSP00000349320.3:p.Lys678Gln
ENST00000443883.1:c.564A>C
NM_000722.3:c.2032A>C NP_000713.2:p.Lys678Gln
XM_005250570.1:c.2068A>C XP_005250627.1:p.Lys690Gln
XM_005250572.1:c.2017A>C XP_005250629.1:p.Lys673Gln
XM_005250573.1:c.2011A>C XP_005250630.1:p.Lys671Gln
XM_005250574.1:c.1996A>C XP_005250631.1:p.Lys666Gln
XM_006716118.1:c.2089A>C XP_006716181.1:p.Lys697Gln
XM_006716119.2:c.2014A>C XP_006716182.1:p.Lys672Gln
XM_006716120.2:c.1972A>C XP_006716183.1:p.Lys658Gln
XM_006716121.2:c.499A>C XP_006716184.1:p.Lys167Gln
XM_011516570.1:c.2089A>C XP_011514872.1:p.Lys697Gln
XM_011516571.1:c.2074A>C XP_011514873.1:p.Lys692Gln
XM_011516572.1:c.2053A>C XP_011514874.1:p.Lys685Gln
XM_011516573.1:c.1858A>C XP_011514875.1:p.Lys620Gln
NM_001366867.1:c.2068A>C NP_001353796.1:p.Lys690Gln
XM_005250572.3:c.2017A>C XP_005250629.1:p.Lys673Gln
XM_005250573.3:c.2011A>C XP_005250630.1:p.Lys671Gln
XM_005250574.3:c.1996A>C XP_005250631.1:p.Lys666Gln
XM_006716118.3:c.2089A>C XP_006716181.1:p.Lys697Gln
XM_006716119.3:c.2014A>C XP_006716182.1:p.Lys672Gln
XM_006716120.3:c.1972A>C XP_006716183.1:p.Lys658Gln
XM_006716121.3:c.499A>C XP_006716184.1:p.Lys167Gln
XM_011516570.3:c.2089A>C XP_011514872.1:p.Lys697Gln
XM_011516571.3:c.2074A>C XP_011514873.1:p.Lys692Gln
XM_011516572.3:c.2053A>C XP_011514874.1:p.Lys685Gln
XM_017012588.1:c.1915A>C XP_016868077.1:p.Lys639Gln
XR_001744873.2:n.2109A>C
XR_001744874.2:n.2016A>C
NM_000722.4:c.2032A>C MANE Select NP_000713.2:p.Lys678Gln