Canonical Allele Identifier: CA10602865
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 280308
ClinVar RCV Id: RCV000322980
dbSNP Id: rs886041537
MyVariant Identifiers: chr3:g.122003165C>G (hg19) chr3:g.122284318C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284318C>G , CM000665.2:g.122284318C>G GRCh38
NC_000003.11:g.122003165C>G , CM000665.1:g.122003165C>G GRCh37
NC_000003.10:g.123485855C>G NCBI36
NG_009058.1:g.105636C>G
NG_009058.2:g.105651C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.2133C>G ENSP00000418685.2:p.Phe711Leu
ENST00000498619.4:c.2394C>G ENSP00000420194.1:p.Phe798Leu
ENST00000638421.1:c.2364C>G ENSP00000492190.1:p.Phe788Leu
ENST00000639785.2:c.2364C>G MANE Select ENSP00000491584.2:p.Phe788Leu
ENST00000490131.5:c.2364C>G ENSP00000418685.1:p.Phe788Leu
ENST00000498619.2:c.2394C>G ENSP00000420194.1:p.Phe798Leu
NM_000388.3:c.2364C>G NP_000379.2:p.Phe788Leu
NM_001178065.1:c.2394C>G NP_001171536.1:p.Phe798Leu
XM_005247836.2:c.2364C>G XP_005247893.1:p.Phe788Leu
XM_005247837.2:c.1881C>G XP_005247894.1:p.Phe627Leu
XM_006713789.2:c.2364C>G XP_006713852.1:p.Phe788Leu
XM_011513237.1:c.2364C>G XP_011511539.1:p.Phe788Leu
XM_011513238.1:c.2364C>G XP_011511540.1:p.Phe788Leu
XM_011513239.1:c.1776C>G XP_011511541.1:p.Phe592Leu
XM_006713789.3:c.2364C>G XP_006713852.1:p.Phe788Leu
XM_017007324.1:c.2364C>G XP_016862813.1:p.Phe788Leu
XM_017007325.1:c.2364C>G XP_016862814.1:p.Phe788Leu
NM_000388.4:c.2364C>G MANE Select NP_000379.3:p.Phe788Leu
NM_001178065.2:c.2394C>G NP_001171536.2:p.Phe798Leu
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