Canonical Allele Identifier: CA2569865

Gene: CASR

Linked Data

• ClinVar Variation Id: 1105757
• ClinVar RCV Id: RCV001430257 ; RCV004038285
• dbSNP Id: rs771142444
• ExAC: 3:122003582 C / G
• gnomAD v2: 3-122003582-C-G
• gnomAD v4: 3-122284735-C-G
• MyVariant Identifiers: chr3:g.122003582C>G (hg19) ; chr3:g.122284735C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284735C>G , CM000665.2:g.122284735C>G	GRCh38
NC_000003.11:g.122003582C>G , CM000665.1:g.122003582C>G	GRCh37
NC_000003.10:g.123486272C>G	NCBI36
NG_009058.1:g.106053C>G
NG_009058.2:g.106068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2550C>G	ENSP00000418685.2:p.Pro850=
ENST00000498619.4:c.2811C>G	ENSP00000420194.1:p.Pro937=
ENST00000638421.1:c.2781C>G	ENSP00000492190.1:p.Pro927=
ENST00000639785.2:c.2781C>G MANE Select	ENSP00000491584.2:p.Pro927=
ENST00000490131.5:c.2781C>G	ENSP00000418685.1:p.Pro927=
ENST00000498619.2:c.2811C>G	ENSP00000420194.1:p.Pro937=
NM_000388.3:c.2781C>G	NP_000379.2:p.Pro927=
NM_001178065.1:c.2811C>G	NP_001171536.1:p.Pro937=
XM_005247836.2:c.2781C>G	XP_005247893.1:p.Pro927=
XM_005247837.2:c.2298C>G	XP_005247894.1:p.Pro766=
XM_006713789.2:c.2781C>G	XP_006713852.1:p.Pro927=
XM_011513237.1:c.2781C>G	XP_011511539.1:p.Pro927=
XM_011513238.1:c.2781C>G	XP_011511540.1:p.Pro927=
XM_011513239.1:c.2193C>G	XP_011511541.1:p.Pro731=
XM_006713789.3:c.2781C>G	XP_006713852.1:p.Pro927=
XM_017007324.1:c.2781C>G	XP_016862813.1:p.Pro927=
XM_017007325.1:c.2781C>G	XP_016862814.1:p.Pro927=
NM_000388.4:c.2781C>G MANE Select	NP_000379.3:p.Pro927=
NM_001178065.2:c.2811C>G	NP_001171536.2:p.Pro937=