Canonical Allele Identifier: CA083346
Community Standard Title: NM_000069.3(CACNA1S):c.4436C>T (p.Thr1479Met)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201048587G>A , CM000663.2:g.201048587G>A GRCh38
NC_000001.10:g.201017715G>A , CM000663.1:g.201017715G>A GRCh37
NC_000001.9:g.199284338G>A NCBI36
NG_009816.1:g.68980C>T
NG_009816.2:g.68980C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4436C>T MANE Select NP_000060.2:p.Thr1479Met
ENST00000362061.4:c.4436C>T MANE Select ENSP00000355192.3:p.Thr1479Met
NM_000069.2:c.4436C>T NP_000060.2:p.Thr1479Met
ENST00000362061.3:c.4436C>T ENSP00000355192.3:p.Thr1479Met
ENST00000367338.7:c.4379C>T ENSP00000356307.3:p.Thr1460Met
ENST00000679417.1:c.*3599C>T ENSP00000506706.1:n.*3599C>T
ENST00000680051.1:n.1562C>T
ENST00000680059.1:c.*1954C>T ENSP00000504944.1:n.*1954C>T
ENST00000681078.1:c.*211C>T ENSP00000506645.1:n.*211C>T
ENST00000681190.1:c.*618C>T ENSP00000506428.1:n.*618C>T
ENST00000681874.1:c.4376C>T ENSP00000505162.1:p.Thr1459Met
XM_005245478.2:c.4379C>T XP_005245535.1:p.Thr1460Met
XM_005245478.3:c.4379C>T XP_005245535.1:p.Thr1460Met