Canonical Allele Identifier: CA2586972875
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284636del , CM000665.2:g.122284636del GRCh38
NC_000003.11:g.122003483del , CM000665.1:g.122003483del GRCh37
NC_000003.10:g.123486173del NCBI36
NG_009058.1:g.105954del
NG_009058.2:g.105969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2451del ENSP00000418685.2:p.Ser818ProfsTer?
ENST00000498619.4:c.2712del ENSP00000420194.1:p.Ser905ProfsTer?
ENST00000638421.1:c.2682del ENSP00000492190.1:p.Ser895ProfsTer?
ENST00000639785.2:c.2682del MANE Select ENSP00000491584.2:p.Ser895ProfsTer?
ENST00000490131.5:c.2682del ENSP00000418685.1:p.Ser895ProfsTer?
ENST00000498619.2:c.2712del ENSP00000420194.1:p.Ser905ProfsTer?
NM_000388.3:c.2682del NP_000379.2:p.Ser895ProfsTer?
NM_001178065.1:c.2712del NP_001171536.1:p.Ser905ProfsTer?
XM_005247836.2:c.2682del XP_005247893.1:p.Ser895ProfsTer?
XM_005247837.2:c.2199del XP_005247894.1:p.Ser734ProfsTer?
XM_006713789.2:c.2682del XP_006713852.1:p.Ser895ProfsTer?
XM_011513237.1:c.2682del XP_011511539.1:p.Ser895ProfsTer?
XM_011513238.1:c.2682del XP_011511540.1:p.Ser895ProfsTer?
XM_011513239.1:c.2094del XP_011511541.1:p.Ser699ProfsTer?
XM_006713789.3:c.2682del XP_006713852.1:p.Ser895ProfsTer?
XM_017007324.1:c.2682del XP_016862813.1:p.Ser895ProfsTer?
XM_017007325.1:c.2682del XP_016862814.1:p.Ser895ProfsTer?
NM_000388.4:c.2682del MANE Select NP_000379.3:p.Ser895ProfsTer?
NM_001178065.2:c.2712del NP_001171536.2:p.Ser905ProfsTer?