Canonical Allele Identifier: CA354161672

Gene: CASR

Linked Data

• ClinVar Variation Id: 532605
• ClinVar RCV Id: RCV000639452
• dbSNP Id: rs1553769334
• MyVariant Identifiers: chr3:g.122003970T>A (hg19) ; chr3:g.122285123T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122285123T>A , CM000665.2:g.122285123T>A	GRCh38
NC_000003.11:g.122003970T>A , CM000665.1:g.122003970T>A	GRCh37
NC_000003.10:g.123486660T>A	NCBI36
NG_009058.1:g.106441T>A
NG_009058.2:g.106456T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2938T>A	ENSP00000418685.2:p.Ser980Thr
ENST00000498619.4:c.3199T>A	ENSP00000420194.1:p.Ser1067Thr
ENST00000638421.1:c.3169T>A	ENSP00000492190.1:p.Ser1057Thr
ENST00000639785.2:c.3169T>A MANE Select	ENSP00000491584.2:p.Ser1057Thr
ENST00000490131.5:c.3169T>A	ENSP00000418685.1:p.Ser1057Thr
ENST00000498619.2:c.3199T>A	ENSP00000420194.1:p.Ser1067Thr
NM_000388.3:c.3169T>A	NP_000379.2:p.Ser1057Thr
NM_001178065.1:c.3199T>A	NP_001171536.1:p.Ser1067Thr
XM_005247836.2:c.3169T>A	XP_005247893.1:p.Ser1057Thr
XM_005247837.2:c.2686T>A	XP_005247894.1:p.Ser896Thr
XM_006713789.2:c.3169T>A	XP_006713852.1:p.Ser1057Thr
XM_011513237.1:c.3169T>A	XP_011511539.1:p.Ser1057Thr
XM_011513238.1:c.3169T>A	XP_011511540.1:p.Ser1057Thr
XM_011513239.1:c.2581T>A	XP_011511541.1:p.Ser861Thr
XM_006713789.3:c.3169T>A	XP_006713852.1:p.Ser1057Thr
XM_017007324.1:c.3169T>A	XP_016862813.1:p.Ser1057Thr
XM_017007325.1:c.3169T>A	XP_016862814.1:p.Ser1057Thr
NM_000388.4:c.3169T>A MANE Select	NP_000379.3:p.Ser1057Thr
NM_001178065.2:c.3199T>A	NP_001171536.2:p.Ser1067Thr