Canonical Allele Identifier: CA083629
Community Standard Title: NM_000069.3(CACNA1S):c.4955G>A (p.Arg1652His)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201043374C>T , CM000663.2:g.201043374C>T GRCh38
NC_000001.10:g.201012502C>T , CM000663.1:g.201012502C>T GRCh37
NC_000001.9:g.199279125C>T NCBI36
NG_009816.1:g.74193G>A
NG_009816.2:g.74193G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4955G>A MANE Select NP_000060.2:p.Arg1652His
ENST00000362061.4:c.4955G>A MANE Select ENSP00000355192.3:p.Arg1652His
NM_000069.2:c.4955G>A NP_000060.2:p.Arg1652His
ENST00000362061.3:c.4955G>A ENSP00000355192.3:p.Arg1652His
ENST00000367338.7:c.4898G>A ENSP00000356307.3:p.Arg1633His
ENST00000679417.1:c.*4118G>A ENSP00000506706.1:n.*4118G>A
ENST00000680051.1:n.2081G>A
ENST00000680059.1:c.*2473G>A ENSP00000504944.1:n.*2473G>A
ENST00000681078.1:c.*730G>A ENSP00000506645.1:n.*730G>A
ENST00000681190.1:c.*1137G>A ENSP00000506428.1:n.*1137G>A
ENST00000681874.1:c.4895G>A ENSP00000505162.1:p.Arg1632His
XM_005245478.2:c.4898G>A XP_005245535.1:p.Arg1633His
XM_005245478.3:c.4898G>A XP_005245535.1:p.Arg1633His