Canonical Allele Identifier: CA083462
Community Standard Title: NM_000069.3(CACNA1S):c.4610T>C (p.Met1537Thr)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201047173A>G , CM000663.2:g.201047173A>G GRCh38
NC_000001.10:g.201016301A>G , CM000663.1:g.201016301A>G GRCh37
NC_000001.9:g.199282924A>G NCBI36
NG_009816.1:g.70394T>C
NG_009816.2:g.70394T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4610T>C MANE Select NP_000060.2:p.Met1537Thr
ENST00000362061.4:c.4610T>C MANE Select ENSP00000355192.3:p.Met1537Thr
NM_000069.2:c.4610T>C NP_000060.2:p.Met1537Thr
ENST00000362061.3:c.4610T>C ENSP00000355192.3:p.Met1537Thr
ENST00000367338.7:c.4553T>C ENSP00000356307.3:p.Met1518Thr
ENST00000679417.1:c.*3773T>C ENSP00000506706.1:n.*3773T>C
ENST00000680051.1:n.1736T>C
ENST00000680059.1:c.*2128T>C ENSP00000504944.1:n.*2128T>C
ENST00000681078.1:c.*385T>C ENSP00000506645.1:n.*385T>C
ENST00000681190.1:c.*792T>C ENSP00000506428.1:n.*792T>C
ENST00000681874.1:c.4550T>C ENSP00000505162.1:p.Met1517Thr
XM_005245478.2:c.4553T>C XP_005245535.1:p.Met1518Thr
XM_005245478.3:c.4553T>C XP_005245535.1:p.Met1518Thr