Canonical Allele Identifier: CA354159631

Gene: CASR

Linked Data

• COSMIC: COSM479299
• MyVariant Identifiers: chr3:g.122003164T>A (hg19) ; chr3:g.122284317T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284317T>A , CM000665.2:g.122284317T>A	GRCh38
NC_000003.11:g.122003164T>A , CM000665.1:g.122003164T>A	GRCh37
NC_000003.10:g.123485854T>A	NCBI36
NG_009058.1:g.105635T>A
NG_009058.2:g.105650T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2132T>A	ENSP00000418685.2:p.Phe711Tyr
ENST00000498619.4:c.2393T>A	ENSP00000420194.1:p.Phe798Tyr
ENST00000638421.1:c.2363T>A	ENSP00000492190.1:p.Phe788Tyr
ENST00000639785.2:c.2363T>A MANE Select	ENSP00000491584.2:p.Phe788Tyr
ENST00000490131.5:c.2363T>A	ENSP00000418685.1:p.Phe788Tyr
ENST00000498619.2:c.2393T>A	ENSP00000420194.1:p.Phe798Tyr
NM_000388.3:c.2363T>A	NP_000379.2:p.Phe788Tyr
NM_001178065.1:c.2393T>A	NP_001171536.1:p.Phe798Tyr
XM_005247836.2:c.2363T>A	XP_005247893.1:p.Phe788Tyr
XM_005247837.2:c.1880T>A	XP_005247894.1:p.Phe627Tyr
XM_006713789.2:c.2363T>A	XP_006713852.1:p.Phe788Tyr
XM_011513237.1:c.2363T>A	XP_011511539.1:p.Phe788Tyr
XM_011513238.1:c.2363T>A	XP_011511540.1:p.Phe788Tyr
XM_011513239.1:c.1775T>A	XP_011511541.1:p.Phe592Tyr
XM_006713789.3:c.2363T>A	XP_006713852.1:p.Phe788Tyr
XM_017007324.1:c.2363T>A	XP_016862813.1:p.Phe788Tyr
XM_017007325.1:c.2363T>A	XP_016862814.1:p.Phe788Tyr
NM_000388.4:c.2363T>A MANE Select	NP_000379.3:p.Phe788Tyr
NM_001178065.2:c.2393T>A	NP_001171536.2:p.Phe798Tyr