Canonical Allele Identifier: CA1397870545

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122257093_122257094delinsTG , CM000665.2:g.122257093_122257094delinsTG	GRCh38
NC_000003.11:g.121975940_121975941delinsTG , CM000665.1:g.121975940_121975941delinsTG	GRCh37
NC_000003.10:g.123458630_123458631delinsTG	NCBI36
NG_009058.1:g.78411_78412delinsTG
NG_009058.2:g.78426_78427delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000490131.7:c.198_199delinsTG	ENSP00000418685.2:p.Arg66=
ENST00000498619.4:c.198_199delinsTG	ENSP00000420194.1:p.Arg66=
ENST00000638296.1:n.117_118delinsTG
ENST00000638421.1:c.198_199delinsTG	ENSP00000492190.1:p.Arg66=
ENST00000639785.2:c.198_199delinsTG MANE Select	ENSP00000491584.2:p.Arg66=
ENST00000490131.5:c.198_199delinsTG	ENSP00000418685.1:p.Arg66=
ENST00000490186.1:n.57_58delinsTG
ENST00000498619.2:c.198_199delinsTG	ENSP00000420194.1:p.Arg66=
NM_000388.3:c.198_199delinsTG	NP_000379.2:p.Arg66=
NM_001178065.1:c.198_199delinsTG	NP_001171536.1:p.Arg66=
XM_005247836.2:c.198_199delinsTG	XP_005247893.1:p.Arg66=
XM_005247837.2:c.9+2719_9+2720delinsTG	XP_005247894.1:n.9+2719_9+2720delinsTG
XM_006713789.2:c.198_199delinsTG	XP_006713852.1:p.Arg66=
XM_011513237.1:c.198_199delinsTG	XP_011511539.1:p.Arg66=
XM_011513238.1:c.198_199delinsTG	XP_011511540.1:p.Arg66=
XM_006713789.3:c.198_199delinsTG	XP_006713852.1:p.Arg66=
XM_017007324.1:c.198_199delinsTG	XP_016862813.1:p.Arg66=
XM_017007325.1:c.198_199delinsTG	XP_016862814.1:p.Arg66=
NM_000388.4:c.198_199delinsTG MANE Select	NP_000379.3:p.Arg66=
NM_001178065.2:c.198_199delinsTG	NP_001171536.2:p.Arg66=