Canonical Allele Identifier: CA2569608
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 237755
dbSNP Id: rs200312817

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122262223A>G , CM000665.2:g.122262223A>G GRCh38
NC_000003.11:g.121981070A>G , CM000665.1:g.121981070A>G GRCh37
NC_000003.10:g.123463760A>G NCBI36
NG_009058.1:g.83541A>G
NG_009058.2:g.83556A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1188A>G ENSP00000418685.2:p.Thr396=
ENST00000498619.4:c.1188A>G ENSP00000420194.1:p.Thr396=
ENST00000638421.1:c.1188A>G ENSP00000492190.1:p.Thr396=
ENST00000639785.2:c.1188A>G MANE Select ENSP00000491584.2:p.Thr396=
ENST00000490131.5:c.1188A>G ENSP00000418685.1:p.Thr396=
ENST00000498619.2:c.1188A>G ENSP00000420194.1:p.Thr396=
NM_000388.3:c.1188A>G NP_000379.2:p.Thr396=
NM_001178065.1:c.1188A>G NP_001171536.1:p.Thr396=
XM_005247836.2:c.1188A>G XP_005247893.1:p.Thr396=
XM_005247837.2:c.705A>G XP_005247894.1:p.Thr235=
XM_006713789.2:c.1188A>G XP_006713852.1:p.Thr396=
XM_011513237.1:c.1188A>G XP_011511539.1:p.Thr396=
XM_011513238.1:c.1188A>G XP_011511540.1:p.Thr396=
XM_011513239.1:c.600A>G XP_011511541.1:p.Thr200=
XM_006713789.3:c.1188A>G XP_006713852.1:p.Thr396=
XM_017007324.1:c.1188A>G XP_016862813.1:p.Thr396=
XM_017007325.1:c.1188A>G XP_016862814.1:p.Thr396=
NM_000388.4:c.1188A>G MANE Select NP_000379.3:p.Thr396=
NM_001178065.2:c.1188A>G NP_001171536.2:p.Thr396=