Canonical Allele Identifier: CA1397872582
Gene: CASR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284539T= , CM000665.2:g.122284539T= GRCh38
NC_000003.11:g.122003386T= , CM000665.1:g.122003386T= GRCh37
NC_000003.10:g.123486076T= NCBI36
NG_009058.1:g.105857T=
NG_009058.2:g.105872T=

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.7:c.2354T= ENSP00000418685.2:p.Phe785=
ENST00000498619.4:c.2615T= ENSP00000420194.1:p.Phe872=
ENST00000638421.1:c.2585T= ENSP00000492190.1:p.Phe862=
ENST00000639785.2:c.2585T= MANE Select ENSP00000491584.2:p.Phe862=
ENST00000490131.5:c.2585T= ENSP00000418685.1:p.Phe862=
ENST00000498619.2:c.2615T= ENSP00000420194.1:p.Phe872=
NM_000388.3:c.2585T= NP_000379.2:p.Phe862=
NM_001178065.1:c.2615T= NP_001171536.1:p.Phe872=
XM_005247836.2:c.2585T= XP_005247893.1:p.Phe862=
XM_005247837.2:c.2102T= XP_005247894.1:p.Phe701=
XM_006713789.2:c.2585T= XP_006713852.1:p.Phe862=
XM_011513237.1:c.2585T= XP_011511539.1:p.Phe862=
XM_011513238.1:c.2585T= XP_011511540.1:p.Phe862=
XM_011513239.1:c.1997T= XP_011511541.1:p.Phe666=
XM_006713789.3:c.2585T= XP_006713852.1:p.Phe862=
XM_017007324.1:c.2585T= XP_016862813.1:p.Phe862=
XM_017007325.1:c.2585T= XP_016862814.1:p.Phe862=
NM_000388.4:c.2585T= MANE Select NP_000379.3:p.Phe862=
NM_001178065.2:c.2615T= NP_001171536.2:p.Phe872=