Canonical Allele Identifier: CA2569545
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 410355
dbSNP Id: rs142745096

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122261883T>C , CM000665.2:g.122261883T>C GRCh38
NC_000003.11:g.121980730T>C , CM000665.1:g.121980730T>C GRCh37
NC_000003.10:g.123463420T>C NCBI36
NG_009058.1:g.83201T>C
NG_009058.2:g.83216T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.848T>C ENSP00000418685.2:p.Ile283Thr
ENST00000498619.4:c.848T>C ENSP00000420194.1:p.Ile283Thr
ENST00000638421.1:c.848T>C ENSP00000492190.1:p.Ile283Thr
ENST00000639785.2:c.848T>C MANE Select ENSP00000491584.2:p.Ile283Thr
ENST00000490131.5:c.848T>C ENSP00000418685.1:p.Ile283Thr
ENST00000498619.2:c.848T>C ENSP00000420194.1:p.Ile283Thr
NM_000388.3:c.848T>C NP_000379.2:p.Ile283Thr
NM_001178065.1:c.848T>C NP_001171536.1:p.Ile283Thr
XM_005247836.2:c.848T>C XP_005247893.1:p.Ile283Thr
XM_005247837.2:c.365T>C XP_005247894.1:p.Ile122Thr
XM_006713789.2:c.848T>C XP_006713852.1:p.Ile283Thr
XM_011513237.1:c.848T>C XP_011511539.1:p.Ile283Thr
XM_011513238.1:c.848T>C XP_011511540.1:p.Ile283Thr
XM_011513239.1:c.260T>C XP_011511541.1:p.Ile87Thr
XM_006713789.3:c.848T>C XP_006713852.1:p.Ile283Thr
XM_017007324.1:c.848T>C XP_016862813.1:p.Ile283Thr
XM_017007325.1:c.848T>C XP_016862814.1:p.Ile283Thr
NM_000388.4:c.848T>C MANE Select NP_000379.3:p.Ile283Thr
NM_001178065.2:c.848T>C NP_001171536.2:p.Ile283Thr