Canonical Allele Identifier: CA083643
Community Standard Title: NM_000069.3(CACNA1S):c.4987A>G (p.Asn1663Asp)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201043342T>C , CM000663.2:g.201043342T>C GRCh38
NC_000001.10:g.201012470T>C , CM000663.1:g.201012470T>C GRCh37
NC_000001.9:g.199279093T>C NCBI36
NG_009816.1:g.74225A>G
NG_009816.2:g.74225A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4987A>G MANE Select NP_000060.2:p.Asn1663Asp
ENST00000362061.4:c.4987A>G MANE Select ENSP00000355192.3:p.Asn1663Asp
NM_000069.2:c.4987A>G NP_000060.2:p.Asn1663Asp
ENST00000362061.3:c.4987A>G ENSP00000355192.3:p.Asn1663Asp
ENST00000367338.7:c.4930A>G ENSP00000356307.3:p.Asn1644Asp
ENST00000679417.1:c.*4150A>G ENSP00000506706.1:n.*4150A>G
ENST00000680051.1:n.2113A>G
ENST00000680059.1:c.*2505A>G ENSP00000504944.1:n.*2505A>G
ENST00000681078.1:c.*762A>G ENSP00000506645.1:n.*762A>G
ENST00000681190.1:c.*1169A>G ENSP00000506428.1:n.*1169A>G
ENST00000681874.1:c.4927A>G ENSP00000505162.1:p.Asn1643Asp
XM_005245478.2:c.4930A>G XP_005245535.1:p.Asn1644Asp
XM_005245478.3:c.4930A>G XP_005245535.1:p.Asn1644Asp