Canonical Allele Identifier: CA898108914
Gene: CASR HGNC NCBI

Linked Data

dbSNP Id: rs1296586326

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122281882_122281884del , CM000665.2:g.122281882_122281884del GRCh38
NC_000003.11:g.122000729_122000731del , CM000665.1:g.122000729_122000731del GRCh37
NC_000003.10:g.123483419_123483421del NCBI36
NG_009058.1:g.103200_103202del
NG_009058.2:g.103215_103217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1378-231_1378-229del ENSP00000418685.2:n.1378-231_1378-229del
ENST00000498619.4:c.1609-201_1609-199del ENSP00000420194.1:n.1609-201_1609-199del
ENST00000638421.1:c.1609-231_1609-229del ENSP00000492190.1:n.1609-231_1609-229del
ENST00000639785.2:c.1609-231_1609-229del MANE Select ENSP00000491584.2:n.1609-231_1609-229del
ENST00000490131.5:c.1609-231_1609-229del ENSP00000418685.1:n.1609-231_1609-229del
ENST00000498619.2:c.1609-201_1609-199del ENSP00000420194.1:n.1609-201_1609-199del
NM_000388.3:c.1609-231_1609-229del NP_000379.2:n.1609-231_1609-229del
NM_001178065.1:c.1609-201_1609-199del NP_001171536.1:n.1609-201_1609-199del
XM_005247836.2:c.1609-231_1609-229del XP_005247893.1:n.1609-231_1609-229del
XM_005247837.2:c.1126-231_1126-229del XP_005247894.1:n.1126-231_1126-229del
XM_006713789.2:c.1609-231_1609-229del XP_006713852.1:n.1609-231_1609-229del
XM_011513237.1:c.1609-231_1609-229del XP_011511539.1:n.1609-231_1609-229del
XM_011513238.1:c.1609-231_1609-229del XP_011511540.1:n.1609-231_1609-229del
XM_011513239.1:c.1021-231_1021-229del XP_011511541.1:n.1021-231_1021-229del
XM_006713789.3:c.1609-231_1609-229del XP_006713852.1:n.1609-231_1609-229del
XM_017007324.1:c.1609-231_1609-229del XP_016862813.1:n.1609-231_1609-229del
XM_017007325.1:c.1609-231_1609-229del XP_016862814.1:n.1609-231_1609-229del
NM_000388.4:c.1609-231_1609-229del MANE Select NP_000379.3:n.1609-231_1609-229del
NM_001178065.2:c.1609-201_1609-199del NP_001171536.2:n.1609-201_1609-199del