Canonical Allele Identifier: CA1397856138
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122254334C= , CM000665.2:g.122254334C= GRCh38
NC_000003.11:g.121973181C= , CM000665.1:g.121973181C= GRCh37
NC_000003.10:g.123455871C= NCBI36
NG_009058.1:g.75652C=
NG_009058.2:g.75667C=

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.145C= ENSP00000418685.2:p.Gln49=
ENST00000498619.4:c.145C= ENSP00000420194.1:p.Gln49=
ENST00000638296.1:n.64C=
ENST00000638421.1:c.145C= ENSP00000492190.1:p.Gln49=
ENST00000639785.2:c.145C= MANE Select ENSP00000491584.2:p.Gln49=
ENST00000490131.5:c.145C= ENSP00000418685.1:p.Gln49=
ENST00000490186.1:n.4C=
ENST00000498619.2:c.145C= ENSP00000420194.1:p.Gln49=
NM_000388.3:c.145C= NP_000379.2:p.Gln49=
NM_001178065.1:c.145C= NP_001171536.1:p.Gln49=
XM_005247836.2:c.145C= XP_005247893.1:p.Gln49=
XM_005247837.2:c.-32C= XP_005247894.1:n.-32C=
XM_006713789.2:c.145C= XP_006713852.1:p.Gln49=
XM_011513237.1:c.145C= XP_011511539.1:p.Gln49=
XM_011513238.1:c.145C= XP_011511540.1:p.Gln49=
XM_006713789.3:c.145C= XP_006713852.1:p.Gln49=
XM_017007324.1:c.145C= XP_016862813.1:p.Gln49=
XM_017007325.1:c.145C= XP_016862814.1:p.Gln49=
NM_000388.4:c.145C= MANE Select NP_000379.3:p.Gln49=
NM_001178065.2:c.145C= NP_001171536.2:p.Gln49=