Canonical Allele Identifier: CA2577870015
Gene: CASR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122261494_122261501del , CM000665.2:g.122261494_122261501del GRCh38
NC_000003.11:g.121980341_121980348del , CM000665.1:g.121980341_121980348del GRCh37
NC_000003.10:g.123463031_123463038del NCBI36
NG_009058.1:g.82812_82819del
NG_009058.2:g.82827_82834del

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.493-34_493-27del ENSP00000418685.2:n.493-34_493-27del
ENST00000498619.4:c.493-34_493-27del ENSP00000420194.1:n.493-34_493-27del
ENST00000638421.1:c.493-34_493-27del ENSP00000492190.1:n.493-34_493-27del
ENST00000639785.2:c.493-34_493-27del MANE Select ENSP00000491584.2:n.493-34_493-27del
ENST00000490131.5:c.493-34_493-27del ENSP00000418685.1:n.493-34_493-27del
ENST00000498619.2:c.493-34_493-27del ENSP00000420194.1:n.493-34_493-27del
NM_000388.3:c.493-34_493-27del NP_000379.2:n.493-34_493-27del
NM_001178065.1:c.493-34_493-27del NP_001171536.1:n.493-34_493-27del
XM_005247836.2:c.493-34_493-27del XP_005247893.1:n.493-34_493-27del
XM_005247837.2:c.10-34_10-27del XP_005247894.1:n.10-34_10-27del
XM_006713789.2:c.493-34_493-27del XP_006713852.1:n.493-34_493-27del
XM_011513237.1:c.493-34_493-27del XP_011511539.1:n.493-34_493-27del
XM_011513238.1:c.493-34_493-27del XP_011511540.1:n.493-34_493-27del
XM_011513239.1:c.-96-34_-96-27del XP_011511541.1:n.-96-34_-96-27del
XM_006713789.3:c.493-34_493-27del XP_006713852.1:n.493-34_493-27del
XM_017007324.1:c.493-34_493-27del XP_016862813.1:n.493-34_493-27del
XM_017007325.1:c.493-34_493-27del XP_016862814.1:n.493-34_493-27del
NM_000388.4:c.493-34_493-27del MANE Select NP_000379.3:n.493-34_493-27del
NM_001178065.2:c.493-34_493-27del NP_001171536.2:n.493-34_493-27del