Canonical Allele Identifier: CA1397871073

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122283836_122283837delinsGC , CM000665.2:g.122283836_122283837delinsGC	GRCh38
NC_000003.11:g.122002683_122002684delinsGC , CM000665.1:g.122002683_122002684delinsGC	GRCh37
NC_000003.10:g.123485373_123485374delinsGC	NCBI36
NG_009058.1:g.105154_105155delinsGC
NG_009058.2:g.105169_105170delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1651_1652delinsGC	ENSP00000418685.2:p.Ala551=
ENST00000498619.4:c.1912_1913delinsGC	ENSP00000420194.1:p.Ala638=
ENST00000638421.1:c.1882_1883delinsGC	ENSP00000492190.1:p.Ala628=
ENST00000639785.2:c.1882_1883delinsGC MANE Select	ENSP00000491584.2:p.Ala628=
ENST00000490131.5:c.1882_1883delinsGC	ENSP00000418685.1:p.Ala628=
ENST00000498619.2:c.1912_1913delinsGC	ENSP00000420194.1:p.Ala638=
NM_000388.3:c.1882_1883delinsGC	NP_000379.2:p.Ala628=
NM_001178065.1:c.1912_1913delinsGC	NP_001171536.1:p.Ala638=
XM_005247836.2:c.1882_1883delinsGC	XP_005247893.1:p.Ala628=
XM_005247837.2:c.1399_1400delinsGC	XP_005247894.1:p.Ala467=
XM_006713789.2:c.1882_1883delinsGC	XP_006713852.1:p.Ala628=
XM_011513237.1:c.1882_1883delinsGC	XP_011511539.1:p.Ala628=
XM_011513238.1:c.1882_1883delinsGC	XP_011511540.1:p.Ala628=
XM_011513239.1:c.1294_1295delinsGC	XP_011511541.1:p.Ala432=
XM_006713789.3:c.1882_1883delinsGC	XP_006713852.1:p.Ala628=
XM_017007324.1:c.1882_1883delinsGC	XP_016862813.1:p.Ala628=
XM_017007325.1:c.1882_1883delinsGC	XP_016862814.1:p.Ala628=
NM_000388.4:c.1882_1883delinsGC MANE Select	NP_000379.3:p.Ala628=
NM_001178065.2:c.1912_1913delinsGC	NP_001171536.2:p.Ala638=