Canonical Allele Identifier: CA354159070

Gene: CASR

Linked Data

• ClinVar Variation Id: 665094
• ClinVar RCV Id: RCV000823304 ; RCV004029139
• dbSNP Id: rs375468610
• MyVariant Identifiers: chr3:g.122003017G>C (hg19) ; chr3:g.122284170G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284170G>C , CM000665.2:g.122284170G>C	GRCh38
NC_000003.11:g.122003017G>C , CM000665.1:g.122003017G>C	GRCh37
NC_000003.10:g.123485707G>C	NCBI36
NG_009058.1:g.105488G>C
NG_009058.2:g.105503G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1985G>C	ENSP00000418685.2:p.Cys662Ser
ENST00000498619.4:c.2246G>C	ENSP00000420194.1:p.Cys749Ser
ENST00000638421.1:c.2216G>C	ENSP00000492190.1:p.Cys739Ser
ENST00000639785.2:c.2216G>C MANE Select	ENSP00000491584.2:p.Cys739Ser
ENST00000490131.5:c.2216G>C	ENSP00000418685.1:p.Cys739Ser
ENST00000498619.2:c.2246G>C	ENSP00000420194.1:p.Cys749Ser
NM_000388.3:c.2216G>C	NP_000379.2:p.Cys739Ser
NM_001178065.1:c.2246G>C	NP_001171536.1:p.Cys749Ser
XM_005247836.2:c.2216G>C	XP_005247893.1:p.Cys739Ser
XM_005247837.2:c.1733G>C	XP_005247894.1:p.Cys578Ser
XM_006713789.2:c.2216G>C	XP_006713852.1:p.Cys739Ser
XM_011513237.1:c.2216G>C	XP_011511539.1:p.Cys739Ser
XM_011513238.1:c.2216G>C	XP_011511540.1:p.Cys739Ser
XM_011513239.1:c.1628G>C	XP_011511541.1:p.Cys543Ser
XM_006713789.3:c.2216G>C	XP_006713852.1:p.Cys739Ser
XM_017007324.1:c.2216G>C	XP_016862813.1:p.Cys739Ser
XM_017007325.1:c.2216G>C	XP_016862814.1:p.Cys739Ser
NM_000388.4:c.2216G>C MANE Select	NP_000379.3:p.Cys739Ser
NM_001178065.2:c.2246G>C	NP_001171536.2:p.Cys749Ser