Canonical Allele Identifier: CA10582121

Gene: CASR

Linked Data

• ClinVar Variation Id: 237757
• ClinVar RCV Id: RCV000230595 ; RCV004020751 ; RCV004554755
• dbSNP Id: rs878853974
• gnomAD v4: 3-122276046-G-T
• MyVariant Identifiers: chr3:g.121994893G>T (hg19) ; chr3:g.122276046G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122276046G>T , CM000665.2:g.122276046G>T	GRCh38
NC_000003.11:g.121994893G>T , CM000665.1:g.121994893G>T	GRCh37
NC_000003.10:g.123477583G>T	NCBI36
NG_009058.1:g.97364G>T
NG_009058.2:g.97379G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1378-6067G>T	ENSP00000418685.2:n.1378-6067G>T
ENST00000498619.4:c.1608+4G>T	ENSP00000420194.1:n.1608+4G>T
ENST00000638421.1:c.1608+4G>T	ENSP00000492190.1:n.1608+4G>T
ENST00000639785.2:c.1608+4G>T MANE Select	ENSP00000491584.2:n.1608+4G>T
ENST00000490131.5:c.1608+4G>T	ENSP00000418685.1:n.1608+4G>T
ENST00000498619.2:c.1608+4G>T	ENSP00000420194.1:n.1608+4G>T
NM_000388.3:c.1608+4G>T	NP_000379.2:n.1608+4G>T
NM_001178065.1:c.1608+4G>T	NP_001171536.1:n.1608+4G>T
XM_005247836.2:c.1608+4G>T	XP_005247893.1:n.1608+4G>T
XM_005247837.2:c.1125+4G>T	XP_005247894.1:n.1125+4G>T
XM_006713789.2:c.1608+4G>T	XP_006713852.1:n.1608+4G>T
XM_011513237.1:c.1608+4G>T	XP_011511539.1:n.1608+4G>T
XM_011513238.1:c.1608+4G>T	XP_011511540.1:n.1608+4G>T
XM_011513239.1:c.1020+4G>T	XP_011511541.1:n.1020+4G>T
XM_006713789.3:c.1608+4G>T	XP_006713852.1:n.1608+4G>T
XM_017007324.1:c.1608+4G>T	XP_016862813.1:n.1608+4G>T
XM_017007325.1:c.1608+4G>T	XP_016862814.1:n.1608+4G>T
NM_000388.4:c.1608+4G>T MANE Select	NP_000379.3:n.1608+4G>T
NM_001178065.2:c.1608+4G>T	NP_001171536.2:n.1608+4G>T