Canonical Allele Identifier: CA2582819224
Gene: CACNA1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235894_13235895del , CM000681.2:g.13235894_13235895del GRCh38
NC_000019.9:g.13346708_13346709del , CM000681.1:g.13346708_13346709del GRCh37
NC_000019.8:g.13207708_13207709del NCBI36
NG_011569.1:g.275566_275567del , LRG_7:g.275566_275567del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.4951-165_4951-164del MANE Select ENSP00000353362.5:n.4951-165_4951-164del
ENST00000573710.7:c.4957-165_4957-164del ENSP00000460092.3:n.4957-165_4957-164del
ENST00000573891.6:c.370-165_370-164del
ENST00000574822.6:n.175-165_175-164del
ENST00000585802.6:c.112-165_112-164del ENSP00000465598.2:n.112-165_112-164del
ENST00000635727.1:c.4954-165_4954-164del ENSP00000490001.1:n.4954-165_4954-164del
ENST00000635742.1:n.940-165_940-164del
ENST00000635895.1:c.4954-165_4954-164del ENSP00000490323.1:n.4954-165_4954-164del
ENST00000636012.1:c.4954-165_4954-164del ENSP00000490223.1:n.4954-165_4954-164del
ENST00000636058.1:c.266-165_266-164del
ENST00000636389.1:c.4954-165_4954-164del ENSP00000489992.1:n.4954-165_4954-164del
ENST00000636473.1:c.112-165_112-164del ENSP00000490173.1:n.112-165_112-164del
ENST00000636549.1:c.4960-165_4960-164del ENSP00000490578.1:n.4960-165_4960-164del
ENST00000637276.1:c.4954-165_4954-164del ENSP00000489777.1:n.4954-165_4954-164del
ENST00000637297.1:c.247-165_247-164del ENSP00000489692.1:n.247-165_247-164del
ENST00000637432.1:c.4969-165_4969-164del ENSP00000490617.1:n.4969-165_4969-164del
ENST00000637736.1:c.4813-165_4813-164del ENSP00000489861.1:n.4813-165_4813-164del
ENST00000637769.1:c.4954-165_4954-164del ENSP00000489778.1:n.4954-165_4954-164del
ENST00000637777.1:c.211-165_211-164del
ENST00000637809.1:n.344-165_344-164del
ENST00000637819.1:c.355-165_355-164del ENSP00000490686.1:n.355-165_355-164del
ENST00000637927.1:c.4957-165_4957-164del ENSP00000489715.1:n.4957-165_4957-164del
ENST00000638009.2:c.4954-165_4954-164del ENSP00000489913.1:n.4954-165_4954-164del
ENST00000638029.1:c.4969-165_4969-164del ENSP00000489829.1:n.4969-165_4969-164del
ENST00000664864.1:c.5155-165_5155-164del ENSP00000499449.1:n.5155-165_5155-164del
ENST00000360228.9:c.4951-165_4951-164del ENSP00000353362.5:n.4951-165_4951-164del
ENST00000573710.6:c.4954-165_4954-164del ENSP00000460092.2:n.4954-165_4954-164del
ENST00000573891.5:c.370-165_370-164del
ENST00000574822.5:n.175-165_175-164del
ENST00000585802.5:c.1009-165_1009-164del ENSP00000465598.1:n.1009-165_1009-164del
ENST00000587525.5:c.412-165_412-164del ENSP00000467729.1:n.412-165_412-164del
ENST00000614285.4:c.4969-165_4969-164del ENSP00000479983.1:n.4969-165_4969-164del
NM_000068.3:c.4969-165_4969-164del NP_000059.3:n.4969-165_4969-164del
NM_001127221.1:c.4954-165_4954-164del , LRG_7t1:c.4954-165_4954-164del NP_001120693.1:n.4954-165_4954-164del
NM_001127222.1:c.4951-165_4951-164del NP_001120694.1:n.4951-165_4951-164del
NM_001174080.1:c.4960-165_4960-164del NP_001167551.1:n.4960-165_4960-164del
NM_023035.2:c.4969-165_4969-164del NP_075461.2:n.4969-165_4969-164del
NM_000068.4:c.4969-165_4969-164del NP_000059.3:n.4969-165_4969-164del
NM_001127222.2:c.4951-165_4951-164del MANE Select NP_001120694.1:n.4951-165_4951-164del
NM_001174080.2:c.4960-165_4960-164del NP_001167551.1:n.4960-165_4960-164del
NM_023035.3:c.4969-165_4969-164del NP_075461.2:n.4969-165_4969-164del
NM_001127221.2:c.4954-165_4954-164del NP_001120693.1:n.4954-165_4954-164del