Canonical Allele Identifier: CA1397885595

Gene: CASR

Linked Data

• dbSNP Id: rs2074889720

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122281675_122281681del , CM000665.2:g.122281675_122281681del	GRCh38
NC_000003.11:g.122000522_122000528del , CM000665.1:g.122000522_122000528del	GRCh37
NC_000003.10:g.123483212_123483218del	NCBI36
NG_009058.1:g.102993_102999del
NG_009058.2:g.103008_103014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1378-438_1378-432del	ENSP00000418685.2:n.1378-438_1378-432del
ENST00000498619.4:c.1609-408_1609-402del	ENSP00000420194.1:n.1609-408_1609-402del
ENST00000638421.1:c.1609-438_1609-432del	ENSP00000492190.1:n.1609-438_1609-432del
ENST00000639785.2:c.1609-438_1609-432del MANE Select	ENSP00000491584.2:n.1609-438_1609-432del
ENST00000490131.5:c.1609-438_1609-432del	ENSP00000418685.1:n.1609-438_1609-432del
ENST00000498619.2:c.1609-408_1609-402del	ENSP00000420194.1:n.1609-408_1609-402del
NM_000388.3:c.1609-438_1609-432del	NP_000379.2:n.1609-438_1609-432del
NM_001178065.1:c.1609-408_1609-402del	NP_001171536.1:n.1609-408_1609-402del
XM_005247836.2:c.1609-438_1609-432del	XP_005247893.1:n.1609-438_1609-432del
XM_005247837.2:c.1126-438_1126-432del	XP_005247894.1:n.1126-438_1126-432del
XM_006713789.2:c.1609-438_1609-432del	XP_006713852.1:n.1609-438_1609-432del
XM_011513237.1:c.1609-438_1609-432del	XP_011511539.1:n.1609-438_1609-432del
XM_011513238.1:c.1609-438_1609-432del	XP_011511540.1:n.1609-438_1609-432del
XM_011513239.1:c.1021-438_1021-432del	XP_011511541.1:n.1021-438_1021-432del
XM_006713789.3:c.1609-438_1609-432del	XP_006713852.1:n.1609-438_1609-432del
XM_017007324.1:c.1609-438_1609-432del	XP_016862813.1:n.1609-438_1609-432del
XM_017007325.1:c.1609-438_1609-432del	XP_016862814.1:n.1609-438_1609-432del
NM_000388.4:c.1609-438_1609-432del MANE Select	NP_000379.3:n.1609-438_1609-432del
NM_001178065.2:c.1609-408_1609-402del	NP_001171536.2:n.1609-408_1609-402del