Canonical Allele Identifier: CA354158996
Gene: CASR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122284153C>G , CM000665.2:g.122284153C>G GRCh38
NC_000003.11:g.122003000C>G , CM000665.1:g.122003000C>G GRCh37
NC_000003.10:g.123485690C>G NCBI36
NG_009058.1:g.105471C>G
NG_009058.2:g.105486C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490131.7:c.1968C>G ENSP00000418685.2:p.Phe656Leu
ENST00000498619.4:c.2229C>G ENSP00000420194.1:p.Phe743Leu
ENST00000638421.1:c.2199C>G ENSP00000492190.1:p.Phe733Leu
ENST00000639785.2:c.2199C>G MANE Select ENSP00000491584.2:p.Phe733Leu
ENST00000490131.5:c.2199C>G ENSP00000418685.1:p.Phe733Leu
ENST00000498619.2:c.2229C>G ENSP00000420194.1:p.Phe743Leu
NM_000388.3:c.2199C>G NP_000379.2:p.Phe733Leu
NM_001178065.1:c.2229C>G NP_001171536.1:p.Phe743Leu
XM_005247836.2:c.2199C>G XP_005247893.1:p.Phe733Leu
XM_005247837.2:c.1716C>G XP_005247894.1:p.Phe572Leu
XM_006713789.2:c.2199C>G XP_006713852.1:p.Phe733Leu
XM_011513237.1:c.2199C>G XP_011511539.1:p.Phe733Leu
XM_011513238.1:c.2199C>G XP_011511540.1:p.Phe733Leu
XM_011513239.1:c.1611C>G XP_011511541.1:p.Phe537Leu
XM_006713789.3:c.2199C>G XP_006713852.1:p.Phe733Leu
XM_017007324.1:c.2199C>G XP_016862813.1:p.Phe733Leu
XM_017007325.1:c.2199C>G XP_016862814.1:p.Phe733Leu
NM_000388.4:c.2199C>G MANE Select NP_000379.3:p.Phe733Leu
NM_001178065.2:c.2229C>G NP_001171536.2:p.Phe743Leu