Canonical Allele Identifier: CA2573136457

Gene: CASR

Linked Data

• ClinVar Variation Id: 1500251
• ClinVar RCV Id: RCV002013385
• dbSNP Id: rs199514129

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122261516G>A , CM000665.2:g.122261516G>A	GRCh38
NC_000003.11:g.121980363G>A , CM000665.1:g.121980363G>A	GRCh37
NC_000003.10:g.123463053G>A	NCBI36
NG_009058.1:g.82834G>A
NG_009058.2:g.82849G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.493-12G>A	ENSP00000418685.2:n.493-12G>A
ENST00000498619.4:c.493-12G>A	ENSP00000420194.1:n.493-12G>A
ENST00000638421.1:c.493-12G>A	ENSP00000492190.1:n.493-12G>A
ENST00000639785.2:c.493-12G>A MANE Select	ENSP00000491584.2:n.493-12G>A
ENST00000490131.5:c.493-12G>A	ENSP00000418685.1:n.493-12G>A
ENST00000498619.2:c.493-12G>A	ENSP00000420194.1:n.493-12G>A
NM_000388.3:c.493-12G>A	NP_000379.2:n.493-12G>A
NM_001178065.1:c.493-12G>A	NP_001171536.1:n.493-12G>A
XM_005247836.2:c.493-12G>A	XP_005247893.1:n.493-12G>A
XM_005247837.2:c.10-12G>A	XP_005247894.1:n.10-12G>A
XM_006713789.2:c.493-12G>A	XP_006713852.1:n.493-12G>A
XM_011513237.1:c.493-12G>A	XP_011511539.1:n.493-12G>A
XM_011513238.1:c.493-12G>A	XP_011511540.1:n.493-12G>A
XM_011513239.1:c.-96-12G>A	XP_011511541.1:n.-96-12G>A
XM_006713789.3:c.493-12G>A	XP_006713852.1:n.493-12G>A
XM_017007324.1:c.493-12G>A	XP_016862813.1:n.493-12G>A
XM_017007325.1:c.493-12G>A	XP_016862814.1:n.493-12G>A
NM_000388.4:c.493-12G>A MANE Select	NP_000379.3:n.493-12G>A
NM_001178065.2:c.493-12G>A	NP_001171536.2:n.493-12G>A