Canonical Allele Identifier: CA435425534
Gene: CASR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.122003645G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284798G>T , CM000665.2:g.122284798G>T GRCh38
NC_000003.11:g.122003645G>T , CM000665.1:g.122003645G>T GRCh37
NC_000003.10:g.123486335G>T NCBI36
NG_009058.1:g.106116G>T
NG_009058.2:g.106131G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.2613G>T ENSP00000418685.2:p.Leu871=
ENST00000498619.4:c.2874G>T ENSP00000420194.1:p.Leu958=
ENST00000638421.1:c.2844G>T ENSP00000492190.1:p.Leu948=
ENST00000639785.2:c.2844G>T MANE Select ENSP00000491584.2:p.Leu948=
ENST00000490131.5:c.2844G>T ENSP00000418685.1:p.Leu948=
ENST00000498619.2:c.2874G>T ENSP00000420194.1:p.Leu958=
NM_000388.3:c.2844G>T NP_000379.2:p.Leu948=
NM_001178065.1:c.2874G>T NP_001171536.1:p.Leu958=
XM_005247836.2:c.2844G>T XP_005247893.1:p.Leu948=
XM_005247837.2:c.2361G>T XP_005247894.1:p.Leu787=
XM_006713789.2:c.2844G>T XP_006713852.1:p.Leu948=
XM_011513237.1:c.2844G>T XP_011511539.1:p.Leu948=
XM_011513238.1:c.2844G>T XP_011511540.1:p.Leu948=
XM_011513239.1:c.2256G>T XP_011511541.1:p.Leu752=
XM_006713789.3:c.2844G>T XP_006713852.1:p.Leu948=
XM_017007324.1:c.2844G>T XP_016862813.1:p.Leu948=
XM_017007325.1:c.2844G>T XP_016862814.1:p.Leu948=
NM_000388.4:c.2844G>T MANE Select NP_000379.3:p.Leu948=
NM_001178065.2:c.2874G>T NP_001171536.2:p.Leu958=