Canonical Allele Identifier: CA1397872747
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122261406G= , CM000665.2:g.122261406G= GRCh38
NC_000003.11:g.121980253G= , CM000665.1:g.121980253G= GRCh37
NC_000003.10:g.123462943G= NCBI36
NG_009058.1:g.82724G=
NG_009058.2:g.82739G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.493-122G= ENSP00000418685.2:n.493-122G=
ENST00000498619.4:c.493-122G= ENSP00000420194.1:n.493-122G=
ENST00000638421.1:c.493-122G= ENSP00000492190.1:n.493-122G=
ENST00000639785.2:c.493-122G= MANE Select ENSP00000491584.2:n.493-122G=
ENST00000490131.5:c.493-122G= ENSP00000418685.1:n.493-122G=
ENST00000498619.2:c.493-122G= ENSP00000420194.1:n.493-122G=
NM_000388.3:c.493-122G= NP_000379.2:n.493-122G=
NM_001178065.1:c.493-122G= NP_001171536.1:n.493-122G=
XM_005247836.2:c.493-122G= XP_005247893.1:n.493-122G=
XM_005247837.2:c.10-122G= XP_005247894.1:n.10-122G=
XM_006713789.2:c.493-122G= XP_006713852.1:n.493-122G=
XM_011513237.1:c.493-122G= XP_011511539.1:n.493-122G=
XM_011513238.1:c.493-122G= XP_011511540.1:n.493-122G=
XM_011513239.1:c.-96-122G= XP_011511541.1:n.-96-122G=
XM_006713789.3:c.493-122G= XP_006713852.1:n.493-122G=
XM_017007324.1:c.493-122G= XP_016862813.1:n.493-122G=
XM_017007325.1:c.493-122G= XP_016862814.1:n.493-122G=
NM_000388.4:c.493-122G= MANE Select NP_000379.3:n.493-122G=
NM_001178065.2:c.493-122G= NP_001171536.2:n.493-122G=