Canonical Allele Identifier: CA216118

Gene: CASR

Linked Data

• ClinVar Variation Id: 64427
• ClinVar RCV Id: RCV000054614 ; RCV001083262 ; RCV001818230 ; RCV004018970 ; RCV002255127
• dbSNP Id: rs201177696
• ExAC: 3:121981074 G / A
• gnomAD v2: 3-121981074-G-A
• gnomAD v3: 3-122262227-G-A
• gnomAD v4: 3-122262227-G-A
• MyVariant Identifiers: chr3:g.121981074G>A (hg19) ; chr3:g.122262227G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122262227G>A , CM000665.2:g.122262227G>A	GRCh38
NC_000003.11:g.121981074G>A , CM000665.1:g.121981074G>A	GRCh37
NC_000003.10:g.123463764G>A	NCBI36
NG_009058.1:g.83545G>A
NG_009058.2:g.83560G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1192G>A	ENSP00000418685.2:p.Asp398Asn
ENST00000498619.4:c.1192G>A	ENSP00000420194.1:p.Asp398Asn
ENST00000638421.1:c.1192G>A	ENSP00000492190.1:p.Asp398Asn
ENST00000639785.2:c.1192G>A MANE Select	ENSP00000491584.2:p.Asp398Asn
ENST00000490131.5:c.1192G>A	ENSP00000418685.1:p.Asp398Asn
ENST00000498619.2:c.1192G>A	ENSP00000420194.1:p.Asp398Asn
NM_000388.3:c.1192G>A	NP_000379.2:p.Asp398Asn
NM_001178065.1:c.1192G>A	NP_001171536.1:p.Asp398Asn
XM_005247836.2:c.1192G>A	XP_005247893.1:p.Asp398Asn
XM_005247837.2:c.709G>A	XP_005247894.1:p.Asp237Asn
XM_006713789.2:c.1192G>A	XP_006713852.1:p.Asp398Asn
XM_011513237.1:c.1192G>A	XP_011511539.1:p.Asp398Asn
XM_011513238.1:c.1192G>A	XP_011511540.1:p.Asp398Asn
XM_011513239.1:c.604G>A	XP_011511541.1:p.Asp202Asn
XM_006713789.3:c.1192G>A	XP_006713852.1:p.Asp398Asn
XM_017007324.1:c.1192G>A	XP_016862813.1:p.Asp398Asn
XM_017007325.1:c.1192G>A	XP_016862814.1:p.Asp398Asn
NM_000388.4:c.1192G>A MANE Select	NP_000379.3:p.Asp398Asn
NM_001178065.2:c.1192G>A	NP_001171536.2:p.Asp398Asn