Canonical Allele Identifier: CA404344492
Community Standard Title: NM_001127222.2(CACNA1A):c.2000A>C (p.Glu667Ala)
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13303871T>G , CM000681.2:g.13303871T>G GRCh38
NC_000019.9:g.13414685T>G , CM000681.1:g.13414685T>G GRCh37
NC_000019.8:g.13275685T>G NCBI36
NG_011569.1:g.207590A>C , LRG_7:g.207590A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001127222.2:c.2000A>C MANE Select NP_001120694.1:p.Glu667Ala
ENST00000360228.11:c.2000A>C MANE Select ENSP00000353362.5:p.Glu667Ala
NM_000068.3:c.2003A>C NP_000059.3:p.Glu668Ala
NM_000068.4:c.2003A>C NP_000059.3:p.Glu668Ala
NM_001127221.1:c.2003A>C , LRG_7t1:c.2003A>C NP_001120693.1:p.Glu668Ala
NM_001127221.2:c.2003A>C NP_001120693.1:p.Glu668Ala
NM_001127222.1:c.2000A>C NP_001120694.1:p.Glu667Ala
NM_001174080.1:c.2003A>C NP_001167551.1:p.Glu668Ala
NM_001174080.2:c.2003A>C NP_001167551.1:p.Glu668Ala
NM_023035.2:c.2003A>C NP_075461.2:p.Glu668Ala
NM_023035.3:c.2003A>C NP_075461.2:p.Glu668Ala
ENST00000360228.9:c.2000A>C ENSP00000353362.5:p.Glu667Ala
ENST00000573710.6:c.2003A>C ENSP00000460092.2:p.Glu668Ala
ENST00000573710.7:c.2006A>C ENSP00000460092.3:p.Glu669Ala
ENST00000614285.4:c.2003A>C ENSP00000479983.1:p.Glu668Ala
ENST00000635727.1:c.2003A>C ENSP00000490001.1:p.Glu668Ala
ENST00000635895.1:c.2003A>C ENSP00000490323.1:p.Glu668Ala
ENST00000636012.1:c.2003A>C ENSP00000490223.1:p.Glu668Ala
ENST00000636389.1:c.2003A>C ENSP00000489992.1:p.Glu668Ala
ENST00000636549.1:c.2003A>C ENSP00000490578.1:p.Glu668Ala
ENST00000637276.1:c.2003A>C ENSP00000489777.1:p.Glu668Ala
ENST00000637432.1:c.2003A>C ENSP00000490617.1:p.Glu668Ala
ENST00000637736.1:c.1862A>C ENSP00000489861.1:p.Glu621Ala
ENST00000637769.1:c.2003A>C ENSP00000489778.1:p.Glu668Ala
ENST00000637927.1:c.2006A>C ENSP00000489715.1:p.Glu669Ala
ENST00000638009.2:c.2003A>C ENSP00000489913.1:p.Glu668Ala
ENST00000638029.1:c.2003A>C ENSP00000489829.1:p.Glu668Ala
ENST00000664864.1:c.2198A>C ENSP00000499449.1:p.Glu733Ala