Canonical Allele Identifier: CA079098
Community Standard Title: NM_000069.3(CACNA1S):c.258+6A>G
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201110158T>C , CM000663.2:g.201110158T>C GRCh38
NC_000001.10:g.201079286T>C , CM000663.1:g.201079286T>C GRCh37
NC_000001.9:g.199345909T>C NCBI36
NG_009816.1:g.7409A>G
NG_009816.2:g.7409A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.258+6A>G MANE Select NP_000060.2:n.258+6A>G
ENST00000362061.4:c.258+6A>G MANE Select ENSP00000355192.3:n.258+6A>G
NM_000069.2:c.258+6A>G NP_000060.2:n.258+6A>G
ENST00000362061.3:c.258+6A>G ENSP00000355192.3:n.258+6A>G
ENST00000367338.7:c.258+6A>G ENSP00000356307.3:n.258+6A>G
ENST00000679417.1:c.258+6A>G ENSP00000506706.1:n.258+6A>G
ENST00000680059.1:c.258+6A>G ENSP00000504944.1:n.258+6A>G
ENST00000681078.1:c.258+6A>G ENSP00000506645.1:n.258+6A>G
ENST00000681190.1:c.258+6A>G ENSP00000506428.1:n.258+6A>G
ENST00000681874.1:c.258+6A>G ENSP00000505162.1:n.258+6A>G
XM_005245478.2:c.258+6A>G XP_005245535.1:n.258+6A>G
XM_005245478.3:c.258+6A>G XP_005245535.1:n.258+6A>G