Canonical Allele Identifier: CA354160835
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 999136
dbSNP Id: rs1293909274

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284773A>C , CM000665.2:g.122284773A>C GRCh38
NC_000003.11:g.122003620A>C , CM000665.1:g.122003620A>C GRCh37
NC_000003.10:g.123486310A>C NCBI36
NG_009058.1:g.106091A>C
NG_009058.2:g.106106A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2588A>C ENSP00000418685.2:p.Gln863Pro
ENST00000498619.4:c.2849A>C ENSP00000420194.1:p.Gln950Pro
ENST00000638421.1:c.2819A>C ENSP00000492190.1:p.Gln940Pro
ENST00000639785.2:c.2819A>C MANE Select ENSP00000491584.2:p.Gln940Pro
ENST00000490131.5:c.2819A>C ENSP00000418685.1:p.Gln940Pro
ENST00000498619.2:c.2849A>C ENSP00000420194.1:p.Gln950Pro
NM_000388.3:c.2819A>C NP_000379.2:p.Gln940Pro
NM_001178065.1:c.2849A>C NP_001171536.1:p.Gln950Pro
XM_005247836.2:c.2819A>C XP_005247893.1:p.Gln940Pro
XM_005247837.2:c.2336A>C XP_005247894.1:p.Gln779Pro
XM_006713789.2:c.2819A>C XP_006713852.1:p.Gln940Pro
XM_011513237.1:c.2819A>C XP_011511539.1:p.Gln940Pro
XM_011513238.1:c.2819A>C XP_011511540.1:p.Gln940Pro
XM_011513239.1:c.2231A>C XP_011511541.1:p.Gln744Pro
XM_006713789.3:c.2819A>C XP_006713852.1:p.Gln940Pro
XM_017007324.1:c.2819A>C XP_016862813.1:p.Gln940Pro
XM_017007325.1:c.2819A>C XP_016862814.1:p.Gln940Pro
NM_000388.4:c.2819A>C MANE Select NP_000379.3:p.Gln940Pro
NM_001178065.2:c.2849A>C NP_001171536.2:p.Gln950Pro