Canonical Allele Identifier: CA354159548
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1484763
ClinVar RCV Id: RCV002006040
dbSNP Id: rs1479933693

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284286G>A , CM000665.2:g.122284286G>A GRCh38
NC_000003.11:g.122003133G>A , CM000665.1:g.122003133G>A GRCh37
NC_000003.10:g.123485823G>A NCBI36
NG_009058.1:g.105604G>A
NG_009058.2:g.105619G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2101G>A ENSP00000418685.2:p.Gly701Ser
ENST00000498619.4:c.2362G>A ENSP00000420194.1:p.Gly788Ser
ENST00000638421.1:c.2332G>A ENSP00000492190.1:p.Gly778Ser
ENST00000639785.2:c.2332G>A MANE Select ENSP00000491584.2:p.Gly778Ser
ENST00000490131.5:c.2332G>A ENSP00000418685.1:p.Gly778Ser
ENST00000498619.2:c.2362G>A ENSP00000420194.1:p.Gly788Ser
NM_000388.3:c.2332G>A NP_000379.2:p.Gly778Ser
NM_001178065.1:c.2362G>A NP_001171536.1:p.Gly788Ser
XM_005247836.2:c.2332G>A XP_005247893.1:p.Gly778Ser
XM_005247837.2:c.1849G>A XP_005247894.1:p.Gly617Ser
XM_006713789.2:c.2332G>A XP_006713852.1:p.Gly778Ser
XM_011513237.1:c.2332G>A XP_011511539.1:p.Gly778Ser
XM_011513238.1:c.2332G>A XP_011511540.1:p.Gly778Ser
XM_011513239.1:c.1744G>A XP_011511541.1:p.Gly582Ser
XM_006713789.3:c.2332G>A XP_006713852.1:p.Gly778Ser
XM_017007324.1:c.2332G>A XP_016862813.1:p.Gly778Ser
XM_017007325.1:c.2332G>A XP_016862814.1:p.Gly778Ser
NM_000388.4:c.2332G>A MANE Select NP_000379.3:p.Gly778Ser
NM_001178065.2:c.2362G>A NP_001171536.2:p.Gly788Ser