Canonical Allele Identifier: CA1397873159

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284984_122284985delinsCG , CM000665.2:g.122284984_122284985delinsCG	GRCh38
NC_000003.11:g.122003831_122003832delinsCG , CM000665.1:g.122003831_122003832delinsCG	GRCh37
NC_000003.10:g.123486521_123486522delinsCG	NCBI36
NG_009058.2:g.106317_106318delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2799_2800delinsCG	ENSP00000418685.2:p.His933=
ENST00000498619.4:c.3060_3061delinsCG	ENSP00000420194.1:p.His1020=
ENST00000638421.1:c.3030_3031delinsCG	ENSP00000492190.1:p.His1010=
ENST00000639785.2:c.3030_3031delinsCG MANE Select	ENSP00000491584.2:p.His1010=
ENST00000490131.5:c.3030_3031delinsCG	ENSP00000418685.1:p.His1010=
ENST00000498619.2:c.3060_3061delinsCG	ENSP00000420194.1:p.His1020=
XM_005247836.2:c.3030_3031delinsCG	XP_005247893.1:p.His1010=
XM_005247837.2:c.2547_2548delinsCG	XP_005247894.1:p.His849=
XM_006713789.2:c.3030_3031delinsCG	XP_006713852.1:p.His1010=
XM_011513237.1:c.3030_3031delinsCG	XP_011511539.1:p.His1010=
XM_011513238.1:c.3030_3031delinsCG	XP_011511540.1:p.His1010=
XM_011513239.1:c.2442_2443delinsCG	XP_011511541.1:p.His814=
XM_006713789.3:c.3030_3031delinsCG	XP_006713852.1:p.His1010=
XM_017007324.1:c.3030_3031delinsCG	XP_016862813.1:p.His1010=
XM_017007325.1:c.3030_3031delinsCG	XP_016862814.1:p.His1010=
NM_000388.4:c.3030_3031delinsCG MANE Select	NP_000379.3:p.His1010=
NM_001178065.2:c.3060_3061delinsCG	NP_001171536.2:p.His1020=