Canonical Allele Identifier: CA1397885631
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122281752T= , CM000665.2:g.122281752T= GRCh38
NC_000003.11:g.122000599T= , CM000665.1:g.122000599T= GRCh37
NC_000003.10:g.123483289T= NCBI36
NG_009058.1:g.103070T=
NG_009058.2:g.103085T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1378-361T= ENSP00000418685.2:n.1378-361T=
ENST00000498619.4:c.1609-331T= ENSP00000420194.1:n.1609-331T=
ENST00000638421.1:c.1609-361T= ENSP00000492190.1:n.1609-361T=
ENST00000639785.2:c.1609-361T= MANE Select ENSP00000491584.2:n.1609-361T=
ENST00000490131.5:c.1609-361T= ENSP00000418685.1:n.1609-361T=
ENST00000498619.2:c.1609-331T= ENSP00000420194.1:n.1609-331T=
NM_000388.3:c.1609-361T= NP_000379.2:n.1609-361T=
NM_001178065.1:c.1609-331T= NP_001171536.1:n.1609-331T=
XM_005247836.2:c.1609-361T= XP_005247893.1:n.1609-361T=
XM_005247837.2:c.1126-361T= XP_005247894.1:n.1126-361T=
XM_006713789.2:c.1609-361T= XP_006713852.1:n.1609-361T=
XM_011513237.1:c.1609-361T= XP_011511539.1:n.1609-361T=
XM_011513238.1:c.1609-361T= XP_011511540.1:n.1609-361T=
XM_011513239.1:c.1021-361T= XP_011511541.1:n.1021-361T=
XM_006713789.3:c.1609-361T= XP_006713852.1:n.1609-361T=
XM_017007324.1:c.1609-361T= XP_016862813.1:n.1609-361T=
XM_017007325.1:c.1609-361T= XP_016862814.1:n.1609-361T=
NM_000388.4:c.1609-361T= MANE Select NP_000379.3:n.1609-361T=
NM_001178065.2:c.1609-331T= NP_001171536.2:n.1609-331T=