Canonical Allele Identifier: CA079528
Community Standard Title: NM_000069.3(CACNA1S):c.3054G>A (p.Gln1018=)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201061468C>T , CM000663.2:g.201061468C>T GRCh38
NC_000001.10:g.201030596C>T , CM000663.1:g.201030596C>T GRCh37
NC_000001.9:g.199297219C>T NCBI36
NG_009816.1:g.56099G>A
NG_009816.2:g.56099G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.3054G>A MANE Select NP_000060.2:p.Gln1018=
ENST00000362061.4:c.3054G>A MANE Select ENSP00000355192.3:p.Gln1018=
NM_000069.2:c.3054G>A NP_000060.2:p.Gln1018=
ENST00000362061.3:c.3054G>A ENSP00000355192.3:p.Gln1018=
ENST00000367338.7:c.3054G>A ENSP00000356307.3:p.Gln1018=
ENST00000679417.1:c.*2217G>A ENSP00000506706.1:n.*2217G>A
ENST00000680051.1:n.180G>A
ENST00000680059.1:c.*572G>A ENSP00000504944.1:n.*572G>A
ENST00000681078.1:c.3054G>A ENSP00000506645.1:p.Gln1018=
ENST00000681190.1:c.3054G>A ENSP00000506428.1:p.Gln1018=
ENST00000681874.1:c.2994G>A ENSP00000505162.1:p.Gln998=
XM_005245478.2:c.3054G>A XP_005245535.1:p.Gln1018=
XM_005245478.3:c.3054G>A XP_005245535.1:p.Gln1018=