Canonical Allele Identifier: CA2569453
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 645213
ClinVar RCV Id: RCV000799255
dbSNP Id: rs764023058
COSMIC: COSM581043

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122257170C>T , CM000665.2:g.122257170C>T GRCh38
NC_000003.11:g.121976017C>T , CM000665.1:g.121976017C>T GRCh37
NC_000003.10:g.123458707C>T NCBI36
NG_009058.1:g.78488C>T
NG_009058.2:g.78503C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.275C>T ENSP00000418685.2:p.Thr92Met
ENST00000498619.4:c.275C>T ENSP00000420194.1:p.Thr92Met
ENST00000638296.1:n.194C>T
ENST00000638421.1:c.275C>T ENSP00000492190.1:p.Thr92Met
ENST00000639785.2:c.275C>T MANE Select ENSP00000491584.2:p.Thr92Met
ENST00000490131.5:c.275C>T ENSP00000418685.1:p.Thr92Met
ENST00000490186.1:n.134C>T
ENST00000498619.2:c.275C>T ENSP00000420194.1:p.Thr92Met
NM_000388.3:c.275C>T NP_000379.2:p.Thr92Met
NM_001178065.1:c.275C>T NP_001171536.1:p.Thr92Met
XM_005247836.2:c.275C>T XP_005247893.1:p.Thr92Met
XM_005247837.2:c.9+2796C>T XP_005247894.1:n.9+2796C>T
XM_006713789.2:c.275C>T XP_006713852.1:p.Thr92Met
XM_011513237.1:c.275C>T XP_011511539.1:p.Thr92Met
XM_011513238.1:c.275C>T XP_011511540.1:p.Thr92Met
XM_006713789.3:c.275C>T XP_006713852.1:p.Thr92Met
XM_017007324.1:c.275C>T XP_016862813.1:p.Thr92Met
XM_017007325.1:c.275C>T XP_016862814.1:p.Thr92Met
NM_000388.4:c.275C>T MANE Select NP_000379.3:p.Thr92Met
NM_001178065.2:c.275C>T NP_001171536.2:p.Thr92Met