Canonical Allele Identifier: CA079503
Community Standard Title: NM_000069.3(CACNA1S):c.3053+19C>G
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201061925G>C , CM000663.2:g.201061925G>C GRCh38
NC_000001.10:g.201031053G>C , CM000663.1:g.201031053G>C GRCh37
NC_000001.9:g.199297676G>C NCBI36
NG_009816.1:g.55642C>G
NG_009816.2:g.55642C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.3053+19C>G MANE Select NP_000060.2:n.3053+19C>G
ENST00000362061.4:c.3053+19C>G MANE Select ENSP00000355192.3:n.3053+19C>G
NM_000069.2:c.3053+19C>G NP_000060.2:n.3053+19C>G
ENST00000362061.3:c.3053+19C>G ENSP00000355192.3:n.3053+19C>G
ENST00000367338.7:c.3053+19C>G ENSP00000356307.3:n.3053+19C>G
ENST00000679417.1:c.*2216+19C>G ENSP00000506706.1:n.*2216+19C>G
ENST00000680051.1:n.179+19C>G
ENST00000680059.1:c.*571+19C>G ENSP00000504944.1:n.*571+19C>G
ENST00000681078.1:c.3053+19C>G ENSP00000506645.1:n.3053+19C>G
ENST00000681190.1:c.3053+19C>G ENSP00000506428.1:n.3053+19C>G
ENST00000681874.1:c.2993+19C>G ENSP00000505162.1:n.2993+19C>G
XM_005245478.2:c.3053+19C>G XP_005245535.1:n.3053+19C>G
XM_005245478.3:c.3053+19C>G XP_005245535.1:n.3053+19C>G