Canonical Allele Identifier: CA1397883109
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122275862G= , CM000665.2:g.122275862G= GRCh38
NC_000003.11:g.121994709G= , CM000665.1:g.121994709G= GRCh37
NC_000003.10:g.123477399G= NCBI36
NG_009058.1:g.97180G=
NG_009058.2:g.97195G=

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.1378-6251G= ENSP00000418685.2:n.1378-6251G=
ENST00000498619.4:c.1428G= ENSP00000420194.1:p.Gln476=
ENST00000638421.1:c.1428G= ENSP00000492190.1:p.Gln476=
ENST00000639785.2:c.1428G= MANE Select ENSP00000491584.2:p.Gln476=
ENST00000490131.5:c.1428G= ENSP00000418685.1:p.Gln476=
ENST00000498619.2:c.1428G= ENSP00000420194.1:p.Gln476=
NM_000388.3:c.1428G= NP_000379.2:p.Gln476=
NM_001178065.1:c.1428G= NP_001171536.1:p.Gln476=
XM_005247836.2:c.1428G= XP_005247893.1:p.Gln476=
XM_005247837.2:c.945G= XP_005247894.1:p.Gln315=
XM_006713789.2:c.1428G= XP_006713852.1:p.Gln476=
XM_011513237.1:c.1428G= XP_011511539.1:p.Gln476=
XM_011513238.1:c.1428G= XP_011511540.1:p.Gln476=
XM_011513239.1:c.840G= XP_011511541.1:p.Gln280=
XM_006713789.3:c.1428G= XP_006713852.1:p.Gln476=
XM_017007324.1:c.1428G= XP_016862813.1:p.Gln476=
XM_017007325.1:c.1428G= XP_016862814.1:p.Gln476=
NM_000388.4:c.1428G= MANE Select NP_000379.3:p.Gln476=
NM_001178065.2:c.1428G= NP_001171536.2:p.Gln476=