Canonical Allele Identifier: CA1397870430

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122257637T= , CM000665.2:g.122257637T=	GRCh38
NC_000003.11:g.121976484T= , CM000665.1:g.121976484T=	GRCh37
NC_000003.10:g.123459174T=	NCBI36
NG_009058.1:g.78955T=
NG_009058.2:g.78970T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.492+250T=	ENSP00000418685.2:n.492+250T=
ENST00000498619.4:c.492+250T=	ENSP00000420194.1:n.492+250T=
ENST00000638296.1:n.661T=
ENST00000638421.1:c.492+250T=	ENSP00000492190.1:n.492+250T=
ENST00000639785.2:c.492+250T= MANE Select	ENSP00000491584.2:n.492+250T=
ENST00000490131.5:c.492+250T=	ENSP00000418685.1:n.492+250T=
ENST00000490186.1:n.601T=
ENST00000498619.2:c.492+250T=	ENSP00000420194.1:n.492+250T=
NM_000388.3:c.492+250T=	NP_000379.2:n.492+250T=
NM_001178065.1:c.492+250T=	NP_001171536.1:n.492+250T=
XM_005247836.2:c.492+250T=	XP_005247893.1:n.492+250T=
XM_005247837.2:c.9+3263T=	XP_005247894.1:n.9+3263T=
XM_006713789.2:c.492+250T=	XP_006713852.1:n.492+250T=
XM_011513237.1:c.492+250T=	XP_011511539.1:n.492+250T=
XM_011513238.1:c.492+250T=	XP_011511540.1:n.492+250T=
XM_006713789.3:c.492+250T=	XP_006713852.1:n.492+250T=
XM_017007324.1:c.492+250T=	XP_016862813.1:n.492+250T=
XM_017007325.1:c.492+250T=	XP_016862814.1:n.492+250T=
NM_000388.4:c.492+250T= MANE Select	NP_000379.3:n.492+250T=
NM_001178065.2:c.492+250T=	NP_001171536.2:n.492+250T=