Canonical Allele Identifier: CA2569889
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 342802
dbSNP Id: rs200620134

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284869C>T , CM000665.2:g.122284869C>T GRCh38
NC_000003.11:g.122003716C>T , CM000665.1:g.122003716C>T GRCh37
NC_000003.10:g.123486406C>T NCBI36
NG_009058.1:g.106187C>T
NG_009058.2:g.106202C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2684C>T ENSP00000418685.2:p.Thr895Met
ENST00000498619.4:c.2945C>T ENSP00000420194.1:p.Thr982Met
ENST00000638421.1:c.2915C>T ENSP00000492190.1:p.Thr972Met
ENST00000639785.2:c.2915C>T MANE Select ENSP00000491584.2:p.Thr972Met
ENST00000490131.5:c.2915C>T ENSP00000418685.1:p.Thr972Met
ENST00000498619.2:c.2945C>T ENSP00000420194.1:p.Thr982Met
NM_000388.3:c.2915C>T NP_000379.2:p.Thr972Met
NM_001178065.1:c.2945C>T NP_001171536.1:p.Thr982Met
XM_005247836.2:c.2915C>T XP_005247893.1:p.Thr972Met
XM_005247837.2:c.2432C>T XP_005247894.1:p.Thr811Met
XM_006713789.2:c.2915C>T XP_006713852.1:p.Thr972Met
XM_011513237.1:c.2915C>T XP_011511539.1:p.Thr972Met
XM_011513238.1:c.2915C>T XP_011511540.1:p.Thr972Met
XM_011513239.1:c.2327C>T XP_011511541.1:p.Thr776Met
XM_006713789.3:c.2915C>T XP_006713852.1:p.Thr972Met
XM_017007324.1:c.2915C>T XP_016862813.1:p.Thr972Met
XM_017007325.1:c.2915C>T XP_016862814.1:p.Thr972Met
NM_000388.4:c.2915C>T MANE Select NP_000379.3:p.Thr972Met
NM_001178065.2:c.2945C>T NP_001171536.2:p.Thr982Met