Canonical Allele Identifier: CA1397874110
Gene: CASR HGNC NCBI

Linked Data

dbSNP Id: rs2074640549

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122262485dup , CM000665.2:g.122262485dup GRCh38
NC_000003.11:g.121981332dup , CM000665.1:g.121981332dup GRCh37
NC_000003.10:g.123464022dup NCBI36
NG_009058.1:g.83803dup
NG_009058.2:g.83818dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1377+73dup ENSP00000418685.2:n.1377+73dup
ENST00000498619.4:c.1377+73dup ENSP00000420194.1:n.1377+73dup
ENST00000638421.1:c.1377+73dup ENSP00000492190.1:n.1377+73dup
ENST00000639785.2:c.1377+73dup MANE Select ENSP00000491584.2:n.1377+73dup
ENST00000490131.5:c.1377+73dup ENSP00000418685.1:n.1377+73dup
ENST00000498619.2:c.1377+73dup ENSP00000420194.1:n.1377+73dup
NM_000388.3:c.1377+73dup NP_000379.2:n.1377+73dup
NM_001178065.1:c.1377+73dup NP_001171536.1:n.1377+73dup
XM_005247836.2:c.1377+73dup XP_005247893.1:n.1377+73dup
XM_005247837.2:c.894+73dup XP_005247894.1:n.894+73dup
XM_006713789.2:c.1377+73dup XP_006713852.1:n.1377+73dup
XM_011513237.1:c.1377+73dup XP_011511539.1:n.1377+73dup
XM_011513238.1:c.1377+73dup XP_011511540.1:n.1377+73dup
XM_011513239.1:c.789+73dup XP_011511541.1:n.789+73dup
XM_006713789.3:c.1377+73dup XP_006713852.1:n.1377+73dup
XM_017007324.1:c.1377+73dup XP_016862813.1:n.1377+73dup
XM_017007325.1:c.1377+73dup XP_016862814.1:n.1377+73dup
NM_000388.4:c.1377+73dup MANE Select NP_000379.3:n.1377+73dup
NM_001178065.2:c.1377+73dup NP_001171536.2:n.1377+73dup