Canonical Allele Identifier: CA1397872808
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284637_122284638delinsTC , CM000665.2:g.122284637_122284638delinsTC GRCh38
NC_000003.11:g.122003484_122003485delinsTC , CM000665.1:g.122003484_122003485delinsTC GRCh37
NC_000003.10:g.123486174_123486175delinsTC NCBI36
NG_009058.1:g.105955_105956delinsTC
NG_009058.2:g.105970_105971delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2452_2453delinsTC ENSP00000418685.2:p.Ser818=
ENST00000498619.4:c.2713_2714delinsTC ENSP00000420194.1:p.Ser905=
ENST00000638421.1:c.2683_2684delinsTC ENSP00000492190.1:p.Ser895=
ENST00000639785.2:c.2683_2684delinsTC MANE Select ENSP00000491584.2:p.Ser895=
ENST00000490131.5:c.2683_2684delinsTC ENSP00000418685.1:p.Ser895=
ENST00000498619.2:c.2713_2714delinsTC ENSP00000420194.1:p.Ser905=
NM_000388.3:c.2683_2684delinsTC NP_000379.2:p.Ser895=
NM_001178065.1:c.2713_2714delinsTC NP_001171536.1:p.Ser905=
XM_005247836.2:c.2683_2684delinsTC XP_005247893.1:p.Ser895=
XM_005247837.2:c.2200_2201delinsTC XP_005247894.1:p.Ser734=
XM_006713789.2:c.2683_2684delinsTC XP_006713852.1:p.Ser895=
XM_011513237.1:c.2683_2684delinsTC XP_011511539.1:p.Ser895=
XM_011513238.1:c.2683_2684delinsTC XP_011511540.1:p.Ser895=
XM_011513239.1:c.2095_2096delinsTC XP_011511541.1:p.Ser699=
XM_006713789.3:c.2683_2684delinsTC XP_006713852.1:p.Ser895=
XM_017007324.1:c.2683_2684delinsTC XP_016862813.1:p.Ser895=
XM_017007325.1:c.2683_2684delinsTC XP_016862814.1:p.Ser895=
NM_000388.4:c.2683_2684delinsTC MANE Select NP_000379.3:p.Ser895=
NM_001178065.2:c.2713_2714delinsTC NP_001171536.2:p.Ser905=