Canonical Allele Identifier: CA435424400

Gene: CASR

Linked Data

• MyVariant Identifiers: chr3:g.121980686G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122261839G>T , CM000665.2:g.122261839G>T	GRCh38
NC_000003.11:g.121980686G>T , CM000665.1:g.121980686G>T	GRCh37
NC_000003.10:g.123463376G>T	NCBI36
NG_009058.1:g.83157G>T
NG_009058.2:g.83172G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.804G>T	ENSP00000418685.2:p.Val268=
ENST00000498619.4:c.804G>T	ENSP00000420194.1:p.Val268=
ENST00000638421.1:c.804G>T	ENSP00000492190.1:p.Val268=
ENST00000639785.2:c.804G>T MANE Select	ENSP00000491584.2:p.Val268=
ENST00000490131.5:c.804G>T	ENSP00000418685.1:p.Val268=
ENST00000498619.2:c.804G>T	ENSP00000420194.1:p.Val268=
NM_000388.3:c.804G>T	NP_000379.2:p.Val268=
NM_001178065.1:c.804G>T	NP_001171536.1:p.Val268=
XM_005247836.2:c.804G>T	XP_005247893.1:p.Val268=
XM_005247837.2:c.321G>T	XP_005247894.1:p.Val107=
XM_006713789.2:c.804G>T	XP_006713852.1:p.Val268=
XM_011513237.1:c.804G>T	XP_011511539.1:p.Val268=
XM_011513238.1:c.804G>T	XP_011511540.1:p.Val268=
XM_011513239.1:c.216G>T	XP_011511541.1:p.Val72=
XM_006713789.3:c.804G>T	XP_006713852.1:p.Val268=
XM_017007324.1:c.804G>T	XP_016862813.1:p.Val268=
XM_017007325.1:c.804G>T	XP_016862814.1:p.Val268=
NM_000388.4:c.804G>T MANE Select	NP_000379.3:p.Val268=
NM_001178065.2:c.804G>T	NP_001171536.2:p.Val268=