Canonical Allele Identifier: CA344102480
Community Standard Title: NM_000069.3(CACNA1S):c.2699G>T (p.Arg900Met)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201066275C>A , CM000663.2:g.201066275C>A GRCh38
NC_000001.10:g.201035403C>A , CM000663.1:g.201035403C>A GRCh37
NC_000001.9:g.199302026C>A NCBI36
NG_009816.1:g.51292G>T
NG_009816.2:g.51292G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.2699G>T MANE Select NP_000060.2:p.Arg900Met
ENST00000362061.4:c.2699G>T MANE Select ENSP00000355192.3:p.Arg900Met
NM_000069.2:c.2699G>T NP_000060.2:p.Arg900Met
ENST00000362061.3:c.2699G>T ENSP00000355192.3:p.Arg900Met
ENST00000367338.7:c.2699G>T ENSP00000356307.3:p.Arg900Met
ENST00000679417.1:c.*1862G>T ENSP00000506706.1:n.*1862G>T
ENST00000680059.1:c.*217G>T ENSP00000504944.1:n.*217G>T
ENST00000681078.1:c.2699G>T ENSP00000506645.1:p.Arg900Met
ENST00000681190.1:c.2699G>T ENSP00000506428.1:p.Arg900Met
ENST00000681874.1:c.2639G>T ENSP00000505162.1:p.Arg880Met
XM_005245478.2:c.2699G>T XP_005245535.1:p.Arg900Met
XM_005245478.3:c.2699G>T XP_005245535.1:p.Arg900Met