Canonical Allele Identifier: CA344120110
Community Standard Title: NM_000069.3(CACNA1S):c.1705T>C (p.Phe569Leu)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201077042A>G , CM000663.2:g.201077042A>G GRCh38
NC_000001.10:g.201046170A>G , CM000663.1:g.201046170A>G GRCh37
NC_000001.9:g.199312793A>G NCBI36
NG_009816.1:g.40525T>C
NG_009816.2:g.40525T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.1705T>C MANE Select NP_000060.2:p.Phe569Leu
ENST00000362061.4:c.1705T>C MANE Select ENSP00000355192.3:p.Phe569Leu
NM_000069.2:c.1705T>C NP_000060.2:p.Phe569Leu
ENST00000362061.3:c.1705T>C ENSP00000355192.3:p.Phe569Leu
ENST00000367338.7:c.1705T>C ENSP00000356307.3:p.Phe569Leu
ENST00000679417.1:c.*868T>C ENSP00000506706.1:n.*868T>C
ENST00000680059.1:c.1705T>C ENSP00000504944.1:p.Phe569Leu
ENST00000681078.1:c.1705T>C ENSP00000506645.1:p.Phe569Leu
ENST00000681190.1:c.1705T>C ENSP00000506428.1:p.Phe569Leu
ENST00000681874.1:c.1705T>C ENSP00000505162.1:p.Phe569Leu
XM_005245478.2:c.1705T>C XP_005245535.1:p.Phe569Leu
XM_005245478.3:c.1705T>C XP_005245535.1:p.Phe569Leu