Canonical Allele Identifier: CA354160502
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 842932
dbSNP Id: rs1057520791

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284611G>A , CM000665.2:g.122284611G>A GRCh38
NC_000003.11:g.122003458G>A , CM000665.1:g.122003458G>A GRCh37
NC_000003.10:g.123486148G>A NCBI36
NG_009058.1:g.105929G>A
NG_009058.2:g.105944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2426G>A ENSP00000418685.2:p.Arg809Gln
ENST00000498619.4:c.2687G>A ENSP00000420194.1:p.Arg896Gln
ENST00000638421.1:c.2657G>A ENSP00000492190.1:p.Arg886Gln
ENST00000639785.2:c.2657G>A MANE Select ENSP00000491584.2:p.Arg886Gln
ENST00000490131.5:c.2657G>A ENSP00000418685.1:p.Arg886Gln
ENST00000498619.2:c.2687G>A ENSP00000420194.1:p.Arg896Gln
NM_000388.3:c.2657G>A NP_000379.2:p.Arg886Gln
NM_001178065.1:c.2687G>A NP_001171536.1:p.Arg896Gln
XM_005247836.2:c.2657G>A XP_005247893.1:p.Arg886Gln
XM_005247837.2:c.2174G>A XP_005247894.1:p.Arg725Gln
XM_006713789.2:c.2657G>A XP_006713852.1:p.Arg886Gln
XM_011513237.1:c.2657G>A XP_011511539.1:p.Arg886Gln
XM_011513238.1:c.2657G>A XP_011511540.1:p.Arg886Gln
XM_011513239.1:c.2069G>A XP_011511541.1:p.Arg690Gln
XM_006713789.3:c.2657G>A XP_006713852.1:p.Arg886Gln
XM_017007324.1:c.2657G>A XP_016862813.1:p.Arg886Gln
XM_017007325.1:c.2657G>A XP_016862814.1:p.Arg886Gln
NM_000388.4:c.2657G>A MANE Select NP_000379.3:p.Arg886Gln
NM_001178065.2:c.2687G>A NP_001171536.2:p.Arg896Gln