Canonical Allele Identifier: CA1397870303

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122256950_122256952delinsCTG , CM000665.2:g.122256950_122256952delinsCTG	GRCh38
NC_000003.11:g.121975797_121975799delinsCTG , CM000665.1:g.121975797_121975799delinsCTG	GRCh37
NC_000003.10:g.123458487_123458489delinsCTG	NCBI36
NG_009058.1:g.78268_78270delinsCTG
NG_009058.2:g.78283_78285delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000490131.7:c.186-131_186-129delinsCTG	ENSP00000418685.2:n.186-131_186-129delinsCTG
ENST00000498619.4:c.186-131_186-129delinsCTG	ENSP00000420194.1:n.186-131_186-129delinsCTG
ENST00000638296.1:n.105-131_105-129delinsCTG
ENST00000638421.1:c.186-131_186-129delinsCTG	ENSP00000492190.1:n.186-131_186-129delinsCTG
ENST00000639785.2:c.186-131_186-129delinsCTG MANE Select	ENSP00000491584.2:n.186-131_186-129delinsCTG
ENST00000490131.5:c.186-131_186-129delinsCTG	ENSP00000418685.1:n.186-131_186-129delinsCTG
ENST00000490186.1:n.45-131_45-129delinsCTG
ENST00000498619.2:c.186-131_186-129delinsCTG	ENSP00000420194.1:n.186-131_186-129delinsCTG
NM_000388.3:c.186-131_186-129delinsCTG	NP_000379.2:n.186-131_186-129delinsCTG
NM_001178065.1:c.186-131_186-129delinsCTG	NP_001171536.1:n.186-131_186-129delinsCTG
XM_005247836.2:c.186-131_186-129delinsCTG	XP_005247893.1:n.186-131_186-129delinsCTG
XM_005247837.2:c.9+2576_9+2578delinsCTG	XP_005247894.1:n.9+2576_9+2578delinsCTG
XM_006713789.2:c.186-131_186-129delinsCTG	XP_006713852.1:n.186-131_186-129delinsCTG
XM_011513237.1:c.186-131_186-129delinsCTG	XP_011511539.1:n.186-131_186-129delinsCTG
XM_011513238.1:c.186-131_186-129delinsCTG	XP_011511540.1:n.186-131_186-129delinsCTG
XM_006713789.3:c.186-131_186-129delinsCTG	XP_006713852.1:n.186-131_186-129delinsCTG
XM_017007324.1:c.186-131_186-129delinsCTG	XP_016862813.1:n.186-131_186-129delinsCTG
XM_017007325.1:c.186-131_186-129delinsCTG	XP_016862814.1:n.186-131_186-129delinsCTG
NM_000388.4:c.186-131_186-129delinsCTG MANE Select	NP_000379.3:n.186-131_186-129delinsCTG
NM_001178065.2:c.186-131_186-129delinsCTG	NP_001171536.2:n.186-131_186-129delinsCTG