Canonical Allele Identifier: CA119493

Gene: CASR

Linked Data

• ClinVar Variation Id: 8327
• ClinVar RCV Id: RCV000008829 ; RCV004018592
• dbSNP Id: rs104893698
• MyVariant Identifiers: chr3:g.122002636T>C (hg19) ; chr3:g.122283789T>C (hg38)
• PubMed: PMID:8813042

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122283789T>C , CM000665.2:g.122283789T>C	GRCh38
NC_000003.11:g.122002636T>C , CM000665.1:g.122002636T>C	GRCh37
NC_000003.10:g.123485326T>C	NCBI36
NG_009058.1:g.105107T>C
NG_009058.2:g.105122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1604T>C	ENSP00000418685.2:p.Phe535Ser
ENST00000498619.4:c.1865T>C	ENSP00000420194.1:p.Phe622Ser
ENST00000638421.1:c.1835T>C	ENSP00000492190.1:p.Phe612Ser
ENST00000639785.2:c.1835T>C MANE Select	ENSP00000491584.2:p.Phe612Ser
ENST00000490131.5:c.1835T>C	ENSP00000418685.1:p.Phe612Ser
ENST00000498619.2:c.1865T>C	ENSP00000420194.1:p.Phe622Ser
NM_000388.3:c.1835T>C	NP_000379.2:p.Phe612Ser
NM_001178065.1:c.1865T>C	NP_001171536.1:p.Phe622Ser
XM_005247836.2:c.1835T>C	XP_005247893.1:p.Phe612Ser
XM_005247837.2:c.1352T>C	XP_005247894.1:p.Phe451Ser
XM_006713789.2:c.1835T>C	XP_006713852.1:p.Phe612Ser
XM_011513237.1:c.1835T>C	XP_011511539.1:p.Phe612Ser
XM_011513238.1:c.1835T>C	XP_011511540.1:p.Phe612Ser
XM_011513239.1:c.1247T>C	XP_011511541.1:p.Phe416Ser
XM_006713789.3:c.1835T>C	XP_006713852.1:p.Phe612Ser
XM_017007324.1:c.1835T>C	XP_016862813.1:p.Phe612Ser
XM_017007325.1:c.1835T>C	XP_016862814.1:p.Phe612Ser
NM_000388.4:c.1835T>C MANE Select	NP_000379.3:p.Phe612Ser
NM_001178065.2:c.1865T>C	NP_001171536.2:p.Phe622Ser