Canonical Allele Identifier: CA422689437

Gene: CACNA1S

Linked Data

• gnomAD v4: 1-201077040-G-A
• MyVariant Identifiers: chr1:g.201046168G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201077040G>A , CM000663.2:g.201077040G>A	GRCh38
NC_000001.10:g.201046168G>A , CM000663.1:g.201046168G>A	GRCh37
NC_000001.9:g.199312791G>A	NCBI36
NG_009816.1:g.40527C>T
NG_009816.2:g.40527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.1707C>T MANE Select	ENSP00000355192.3:p.Phe569=
ENST00000679417.1:c.*870C>T	ENSP00000506706.1:n.*870C>T
ENST00000680059.1:c.1707C>T	ENSP00000504944.1:p.Phe569=
ENST00000681078.1:c.1707C>T	ENSP00000506645.1:p.Phe569=
ENST00000681190.1:c.1707C>T	ENSP00000506428.1:p.Phe569=
ENST00000681874.1:c.1707C>T	ENSP00000505162.1:p.Phe569=
ENST00000362061.3:c.1707C>T	ENSP00000355192.3:p.Phe569=
ENST00000367338.7:c.1707C>T	ENSP00000356307.3:p.Phe569=
NM_000069.2:c.1707C>T	NP_000060.2:p.Phe569=
XM_005245478.2:c.1707C>T	XP_005245535.1:p.Phe569=
XM_005245478.3:c.1707C>T	XP_005245535.1:p.Phe569=
NM_000069.3:c.1707C>T MANE Select	NP_000060.2:p.Phe569=