Canonical Allele Identifier: CA079080
Community Standard Title: NM_000069.3(CACNA1S):c.2555C>T (p.Thr852Met)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201066989G>A , CM000663.2:g.201066989G>A GRCh38
NC_000001.10:g.201036117G>A , CM000663.1:g.201036117G>A GRCh37
NC_000001.9:g.199302740G>A NCBI36
NG_009816.1:g.50578C>T
NG_009816.2:g.50578C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.2555C>T MANE Select NP_000060.2:p.Thr852Met
ENST00000362061.4:c.2555C>T MANE Select ENSP00000355192.3:p.Thr852Met
NM_000069.2:c.2555C>T NP_000060.2:p.Thr852Met
ENST00000362061.3:c.2555C>T ENSP00000355192.3:p.Thr852Met
ENST00000367338.7:c.2555C>T ENSP00000356307.3:p.Thr852Met
ENST00000679417.1:c.*1718C>T ENSP00000506706.1:n.*1718C>T
ENST00000680059.1:c.*73C>T ENSP00000504944.1:n.*73C>T
ENST00000681078.1:c.2555C>T ENSP00000506645.1:p.Thr852Met
ENST00000681190.1:c.2555C>T ENSP00000506428.1:p.Thr852Met
ENST00000681874.1:c.2495C>T ENSP00000505162.1:p.Thr832Met
XM_005245478.2:c.2555C>T XP_005245535.1:p.Thr852Met
XM_005245478.3:c.2555C>T XP_005245535.1:p.Thr852Met