Canonical Allele Identifier: CA354159304

Gene: CASR

Linked Data

• ClinVar Variation Id: 2951821
• ClinVar RCV Id: RCV003812508
• MyVariant Identifiers: chr3:g.122003083T>C (hg19) ; chr3:g.122284236T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284236T>C , CM000665.2:g.122284236T>C	GRCh38
NC_000003.11:g.122003083T>C , CM000665.1:g.122003083T>C	GRCh37
NC_000003.10:g.123485773T>C	NCBI36
NG_009058.1:g.105554T>C
NG_009058.2:g.105569T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2051T>C	ENSP00000418685.2:p.Ile684Thr
ENST00000498619.4:c.2312T>C	ENSP00000420194.1:p.Ile771Thr
ENST00000638421.1:c.2282T>C	ENSP00000492190.1:p.Ile761Thr
ENST00000639785.2:c.2282T>C MANE Select	ENSP00000491584.2:p.Ile761Thr
ENST00000490131.5:c.2282T>C	ENSP00000418685.1:p.Ile761Thr
ENST00000498619.2:c.2312T>C	ENSP00000420194.1:p.Ile771Thr
NM_000388.3:c.2282T>C	NP_000379.2:p.Ile761Thr
NM_001178065.1:c.2312T>C	NP_001171536.1:p.Ile771Thr
XM_005247836.2:c.2282T>C	XP_005247893.1:p.Ile761Thr
XM_005247837.2:c.1799T>C	XP_005247894.1:p.Ile600Thr
XM_006713789.2:c.2282T>C	XP_006713852.1:p.Ile761Thr
XM_011513237.1:c.2282T>C	XP_011511539.1:p.Ile761Thr
XM_011513238.1:c.2282T>C	XP_011511540.1:p.Ile761Thr
XM_011513239.1:c.1694T>C	XP_011511541.1:p.Ile565Thr
XM_006713789.3:c.2282T>C	XP_006713852.1:p.Ile761Thr
XM_017007324.1:c.2282T>C	XP_016862813.1:p.Ile761Thr
XM_017007325.1:c.2282T>C	XP_016862814.1:p.Ile761Thr
NM_000388.4:c.2282T>C MANE Select	NP_000379.3:p.Ile761Thr
NM_001178065.2:c.2312T>C	NP_001171536.2:p.Ile771Thr