Canonical Allele Identifier: CA435251511

Gene: CASR

Linked Data

• MyVariant Identifiers: chr3:g.122001013C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122282166C>A , CM000665.2:g.122282166C>A	GRCh38
NC_000003.11:g.122001013C>A , CM000665.1:g.122001013C>A	GRCh37
NC_000003.10:g.123483703C>A	NCBI36
NG_009058.1:g.103484C>A
NG_009058.2:g.103499C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1431C>A	ENSP00000418685.2:p.Ile477=
ENST00000498619.4:c.1692C>A	ENSP00000420194.1:p.Ile564=
ENST00000638421.1:c.1662C>A	ENSP00000492190.1:p.Ile554=
ENST00000639785.2:c.1662C>A MANE Select	ENSP00000491584.2:p.Ile554=
ENST00000490131.5:c.1662C>A	ENSP00000418685.1:p.Ile554=
ENST00000498619.2:c.1692C>A	ENSP00000420194.1:p.Ile564=
NM_000388.3:c.1662C>A	NP_000379.2:p.Ile554=
NM_001178065.1:c.1692C>A	NP_001171536.1:p.Ile564=
XM_005247836.2:c.1662C>A	XP_005247893.1:p.Ile554=
XM_005247837.2:c.1179C>A	XP_005247894.1:p.Ile393=
XM_006713789.2:c.1662C>A	XP_006713852.1:p.Ile554=
XM_011513237.1:c.1662C>A	XP_011511539.1:p.Ile554=
XM_011513238.1:c.1662C>A	XP_011511540.1:p.Ile554=
XM_011513239.1:c.1074C>A	XP_011511541.1:p.Ile358=
XM_006713789.3:c.1662C>A	XP_006713852.1:p.Ile554=
XM_017007324.1:c.1662C>A	XP_016862813.1:p.Ile554=
XM_017007325.1:c.1662C>A	XP_016862814.1:p.Ile554=
NM_000388.4:c.1662C>A MANE Select	NP_000379.3:p.Ile554=
NM_001178065.2:c.1692C>A	NP_001171536.2:p.Ile564=