Canonical Allele Identifier: CA344121180

Gene: CACNA1S

Linked Data

• MyVariant Identifiers: chr1:g.201047034C>G (hg19) ; chr1:g.201077906C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201077906C>G , CM000663.2:g.201077906C>G	GRCh38
NC_000001.10:g.201047034C>G , CM000663.1:g.201047034C>G	GRCh37
NC_000001.9:g.199313657C>G	NCBI36
NG_009816.1:g.39661G>C
NG_009816.2:g.39661G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.1592G>C MANE Select	ENSP00000355192.3:p.Arg531Pro
ENST00000679417.1:c.*755G>C	ENSP00000506706.1:n.*755G>C
ENST00000680059.1:c.1592G>C	ENSP00000504944.1:p.Arg531Pro
ENST00000681078.1:c.1592G>C	ENSP00000506645.1:p.Arg531Pro
ENST00000681190.1:c.1592G>C	ENSP00000506428.1:p.Arg531Pro
ENST00000681874.1:c.1592G>C	ENSP00000505162.1:p.Arg531Pro
ENST00000362061.3:c.1592G>C	ENSP00000355192.3:p.Arg531Pro
ENST00000367338.7:c.1592G>C	ENSP00000356307.3:p.Arg531Pro
NM_000069.2:c.1592G>C	NP_000060.2:p.Arg531Pro
XM_005245478.2:c.1592G>C	XP_005245535.1:p.Arg531Pro
XM_005245478.3:c.1592G>C	XP_005245535.1:p.Arg531Pro
NM_000069.3:c.1592G>C MANE Select	NP_000060.2:p.Arg531Pro