Canonical Allele Identifier: CA344143483
Community Standard Title: NM_000069.3(CACNA1S):c.4453C>T (p.Gln1485Ter)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201047615G>A , CM000663.2:g.201047615G>A GRCh38
NC_000001.10:g.201016743G>A , CM000663.1:g.201016743G>A GRCh37
NC_000001.9:g.199283366G>A NCBI36
NG_009816.1:g.69952C>T
NG_009816.2:g.69952C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4453C>T MANE Select NP_000060.2:p.Gln1485Ter
ENST00000362061.4:c.4453C>T MANE Select ENSP00000355192.3:p.Gln1485Ter
NM_000069.2:c.4453C>T NP_000060.2:p.Gln1485Ter
ENST00000362061.3:c.4453C>T ENSP00000355192.3:p.Gln1485Ter
ENST00000367338.7:c.4396C>T ENSP00000356307.3:p.Gln1466Ter
ENST00000679417.1:c.*3616C>T ENSP00000506706.1:n.*3616C>T
ENST00000680051.1:n.1579C>T
ENST00000680059.1:c.*1971C>T ENSP00000504944.1:n.*1971C>T
ENST00000681078.1:c.*228C>T ENSP00000506645.1:n.*228C>T
ENST00000681190.1:c.*635C>T ENSP00000506428.1:n.*635C>T
ENST00000681874.1:c.4393C>T ENSP00000505162.1:p.Gln1465Ter
XM_005245478.2:c.4396C>T XP_005245535.1:p.Gln1466Ter
XM_005245478.3:c.4396C>T XP_005245535.1:p.Gln1466Ter