Canonical Allele Identifier: CA1397873574
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122262199_122262200delinsGA , CM000665.2:g.122262199_122262200delinsGA GRCh38
NC_000003.11:g.121981046_121981047delinsGA , CM000665.1:g.121981046_121981047delinsGA GRCh37
NC_000003.10:g.123463736_123463737delinsGA NCBI36
NG_009058.1:g.83517_83518delinsGA
NG_009058.2:g.83532_83533delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1164_1165delinsGA ENSP00000418685.2:p.Ser388=
ENST00000498619.4:c.1164_1165delinsGA ENSP00000420194.1:p.Ser388=
ENST00000638421.1:c.1164_1165delinsGA ENSP00000492190.1:p.Ser388=
ENST00000639785.2:c.1164_1165delinsGA MANE Select ENSP00000491584.2:p.Ser388=
ENST00000490131.5:c.1164_1165delinsGA ENSP00000418685.1:p.Ser388=
ENST00000498619.2:c.1164_1165delinsGA ENSP00000420194.1:p.Ser388=
NM_000388.3:c.1164_1165delinsGA NP_000379.2:p.Ser388=
NM_001178065.1:c.1164_1165delinsGA NP_001171536.1:p.Ser388=
XM_005247836.2:c.1164_1165delinsGA XP_005247893.1:p.Ser388=
XM_005247837.2:c.681_682delinsGA XP_005247894.1:p.Ser227=
XM_006713789.2:c.1164_1165delinsGA XP_006713852.1:p.Ser388=
XM_011513237.1:c.1164_1165delinsGA XP_011511539.1:p.Ser388=
XM_011513238.1:c.1164_1165delinsGA XP_011511540.1:p.Ser388=
XM_011513239.1:c.576_577delinsGA XP_011511541.1:p.Ser192=
XM_006713789.3:c.1164_1165delinsGA XP_006713852.1:p.Ser388=
XM_017007324.1:c.1164_1165delinsGA XP_016862813.1:p.Ser388=
XM_017007325.1:c.1164_1165delinsGA XP_016862814.1:p.Ser388=
NM_000388.4:c.1164_1165delinsGA MANE Select NP_000379.3:p.Ser388=
NM_001178065.2:c.1164_1165delinsGA NP_001171536.2:p.Ser388=