Canonical Allele Identifier: CA083203
Community Standard Title: NM_000069.3(CACNA1S):c.4250T>A (p.Ile1417Asn)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201049091A>T , CM000663.2:g.201049091A>T GRCh38
NC_000001.10:g.201018219A>T , CM000663.1:g.201018219A>T GRCh37
NC_000001.9:g.199284842A>T NCBI36
NG_009816.1:g.68476T>A
NG_009816.2:g.68476T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4250T>A MANE Select NP_000060.2:p.Ile1417Asn
ENST00000362061.4:c.4250T>A MANE Select ENSP00000355192.3:p.Ile1417Asn
NM_000069.2:c.4250T>A NP_000060.2:p.Ile1417Asn
ENST00000362061.3:c.4250T>A ENSP00000355192.3:p.Ile1417Asn
ENST00000367338.7:c.4193T>A ENSP00000356307.3:p.Ile1398Asn
ENST00000679417.1:c.*3413T>A ENSP00000506706.1:n.*3413T>A
ENST00000680051.1:n.1376T>A
ENST00000680059.1:c.*1768T>A ENSP00000504944.1:n.*1768T>A
ENST00000681078.1:c.4250T>A ENSP00000506645.1:p.Ile1417Asn
ENST00000681190.1:c.*432T>A ENSP00000506428.1:n.*432T>A
ENST00000681874.1:c.4190T>A ENSP00000505162.1:p.Ile1397Asn
XM_005245478.2:c.4193T>A XP_005245535.1:p.Ile1398Asn
XM_005245478.3:c.4193T>A XP_005245535.1:p.Ile1398Asn