Canonical Allele Identifier: CA2586972799
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122261528_122261532del , CM000665.2:g.122261528_122261532del GRCh38
NC_000003.11:g.121980375_121980379del , CM000665.1:g.121980375_121980379del GRCh37
NC_000003.10:g.123463065_123463069del NCBI36
NG_009058.1:g.82846_82850del
NG_009058.2:g.82861_82865del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.493_497del
ENST00000498619.4:c.493_497del
ENST00000638421.1:c.493_497del
ENST00000639785.2:c.493_497del
ENST00000490131.5:c.493_497del
ENST00000498619.2:c.493_497del
NM_000388.3:c.493_497del
NM_001178065.1:c.493_497del
XM_005247836.2:c.493_497del
XM_005247837.2:c.10_14del
XM_006713789.2:c.493_497del
XM_011513237.1:c.493_497del
XM_011513238.1:c.493_497del
XM_011513239.1:c.-96_-92del
XM_006713789.3:c.493_497del
XM_017007324.1:c.493_497del
XM_017007325.1:c.493_497del
NM_000388.4:c.493_497del
NM_001178065.2:c.493_497del