Canonical Allele Identifier: CA2569406
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 463950
dbSNP Id: rs199515839

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122254229A>G , CM000665.2:g.122254229A>G GRCh38
NC_000003.11:g.121973076A>G , CM000665.1:g.121973076A>G GRCh37
NC_000003.10:g.123455766A>G NCBI36
NG_009058.1:g.75547A>G
NG_009058.2:g.75562A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.40A>G ENSP00000418685.2:p.Thr14Ala
ENST00000498619.4:c.40A>G ENSP00000420194.1:p.Thr14Ala
ENST00000638421.1:c.40A>G ENSP00000492190.1:p.Thr14Ala
ENST00000639785.2:c.40A>G MANE Select ENSP00000491584.2:p.Thr14Ala
ENST00000490131.5:c.40A>G ENSP00000418685.1:p.Thr14Ala
ENST00000498619.2:c.40A>G ENSP00000420194.1:p.Thr14Ala
NM_000388.3:c.40A>G NP_000379.2:p.Thr14Ala
NM_001178065.1:c.40A>G NP_001171536.1:p.Thr14Ala
XM_005247836.2:c.40A>G XP_005247893.1:p.Thr14Ala
XM_006713789.2:c.40A>G XP_006713852.1:p.Thr14Ala
XM_011513237.1:c.40A>G XP_011511539.1:p.Thr14Ala
XM_011513238.1:c.40A>G XP_011511540.1:p.Thr14Ala
XM_006713789.3:c.40A>G XP_006713852.1:p.Thr14Ala
XM_017007324.1:c.40A>G XP_016862813.1:p.Thr14Ala
XM_017007325.1:c.40A>G XP_016862814.1:p.Thr14Ala
NM_000388.4:c.40A>G MANE Select NP_000379.3:p.Thr14Ala
NM_001178065.2:c.40A>G NP_001171536.2:p.Thr14Ala