Canonical Allele Identifier: CA083133
Community Standard Title: NM_000069.3(CACNA1S):c.4166G>A (p.Arg1389Gln)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201050464C>T , CM000663.2:g.201050464C>T GRCh38
NC_000001.10:g.201019592C>T , CM000663.1:g.201019592C>T GRCh37
NC_000001.9:g.199286215C>T NCBI36
NG_009816.1:g.67103G>A
NG_009816.2:g.67103G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4166G>A MANE Select NP_000060.2:p.Arg1389Gln
ENST00000362061.4:c.4166G>A MANE Select ENSP00000355192.3:p.Arg1389Gln
NM_000069.2:c.4166G>A NP_000060.2:p.Arg1389Gln
ENST00000362061.3:c.4166G>A ENSP00000355192.3:p.Arg1389Gln
ENST00000367338.7:c.4109G>A ENSP00000356307.3:p.Arg1370Gln
ENST00000679417.1:c.*3329G>A ENSP00000506706.1:n.*3329G>A
ENST00000680051.1:n.1292G>A
ENST00000680059.1:c.*1684G>A ENSP00000504944.1:n.*1684G>A
ENST00000681078.1:c.4166G>A ENSP00000506645.1:p.Arg1389Gln
ENST00000681190.1:c.*348G>A ENSP00000506428.1:n.*348G>A
ENST00000681874.1:c.4106G>A ENSP00000505162.1:p.Arg1369Gln
XM_005245478.2:c.4109G>A XP_005245535.1:p.Arg1370Gln
XM_005245478.3:c.4109G>A XP_005245535.1:p.Arg1370Gln