Canonical Allele Identifier: CA083175
Community Standard Title: NM_000069.3(CACNA1S):c.4242-10C>G
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201049109G>C , CM000663.2:g.201049109G>C GRCh38
NC_000001.10:g.201018237G>C , CM000663.1:g.201018237G>C GRCh37
NC_000001.9:g.199284860G>C NCBI36
NG_009816.1:g.68458C>G
NG_009816.2:g.68458C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4242-10C>G MANE Select NP_000060.2:n.4242-10C>G
ENST00000362061.4:c.4242-10C>G MANE Select ENSP00000355192.3:n.4242-10C>G
NM_000069.2:c.4242-10C>G NP_000060.2:n.4242-10C>G
ENST00000362061.3:c.4242-10C>G ENSP00000355192.3:n.4242-10C>G
ENST00000367338.7:c.4185-10C>G ENSP00000356307.3:n.4185-10C>G
ENST00000679417.1:c.*3405-10C>G ENSP00000506706.1:n.*3405-10C>G
ENST00000680051.1:n.1368-10C>G
ENST00000680059.1:c.*1760-10C>G ENSP00000504944.1:n.*1760-10C>G
ENST00000681078.1:c.4242-10C>G ENSP00000506645.1:n.4242-10C>G
ENST00000681190.1:c.*424-10C>G ENSP00000506428.1:n.*424-10C>G
ENST00000681874.1:c.4182-10C>G ENSP00000505162.1:n.4182-10C>G
XM_005245478.2:c.4185-10C>G XP_005245535.1:n.4185-10C>G
XM_005245478.3:c.4185-10C>G XP_005245535.1:n.4185-10C>G