Canonical Allele Identifier: CA1397870346

Gene: CASR

Linked Data

• dbSNP Id: rs2074569344

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122257536T>C , CM000665.2:g.122257536T>C	GRCh38
NC_000003.11:g.121976383T>C , CM000665.1:g.121976383T>C	GRCh37
NC_000003.10:g.123459073T>C	NCBI36
NG_009058.1:g.78854T>C
NG_009058.2:g.78869T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.492+149T>C	ENSP00000418685.2:n.492+149T>C
ENST00000498619.4:c.492+149T>C	ENSP00000420194.1:n.492+149T>C
ENST00000638296.1:n.560T>C
ENST00000638421.1:c.492+149T>C	ENSP00000492190.1:n.492+149T>C
ENST00000639785.2:c.492+149T>C MANE Select	ENSP00000491584.2:n.492+149T>C
ENST00000490131.5:c.492+149T>C	ENSP00000418685.1:n.492+149T>C
ENST00000490186.1:n.500T>C
ENST00000498619.2:c.492+149T>C	ENSP00000420194.1:n.492+149T>C
NM_000388.3:c.492+149T>C	NP_000379.2:n.492+149T>C
NM_001178065.1:c.492+149T>C	NP_001171536.1:n.492+149T>C
XM_005247836.2:c.492+149T>C	XP_005247893.1:n.492+149T>C
XM_005247837.2:c.9+3162T>C	XP_005247894.1:n.9+3162T>C
XM_006713789.2:c.492+149T>C	XP_006713852.1:n.492+149T>C
XM_011513237.1:c.492+149T>C	XP_011511539.1:n.492+149T>C
XM_011513238.1:c.492+149T>C	XP_011511540.1:n.492+149T>C
XM_006713789.3:c.492+149T>C	XP_006713852.1:n.492+149T>C
XM_017007324.1:c.492+149T>C	XP_016862813.1:n.492+149T>C
XM_017007325.1:c.492+149T>C	XP_016862814.1:n.492+149T>C
NM_000388.4:c.492+149T>C MANE Select	NP_000379.3:n.492+149T>C
NM_001178065.2:c.492+149T>C	NP_001171536.2:n.492+149T>C