Canonical Allele Identifier: CA1397871858

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284197_122284198delinsCG , CM000665.2:g.122284197_122284198delinsCG	GRCh38
NC_000003.11:g.122003044_122003045delinsCG , CM000665.1:g.122003044_122003045delinsCG	GRCh37
NC_000003.10:g.123485734_123485735delinsCG	NCBI36
NG_009058.2:g.105530_105531delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2012_2013delinsCG	ENSP00000418685.2:p.Pro671=
ENST00000498619.4:c.2273_2274delinsCG	ENSP00000420194.1:p.Pro758=
ENST00000638421.1:c.2243_2244delinsCG	ENSP00000492190.1:p.Pro748=
ENST00000639785.2:c.2243_2244delinsCG MANE Select	ENSP00000491584.2:p.Pro748=
ENST00000490131.5:c.2243_2244delinsCG	ENSP00000418685.1:p.Pro748=
ENST00000498619.2:c.2273_2274delinsCG	ENSP00000420194.1:p.Pro758=
XM_005247836.2:c.2243_2244delinsCG	XP_005247893.1:p.Pro748=
XM_005247837.2:c.1760_1761delinsCG	XP_005247894.1:p.Pro587=
XM_006713789.2:c.2243_2244delinsCG	XP_006713852.1:p.Pro748=
XM_011513237.1:c.2243_2244delinsCG	XP_011511539.1:p.Pro748=
XM_011513238.1:c.2243_2244delinsCG	XP_011511540.1:p.Pro748=
XM_011513239.1:c.1655_1656delinsCG	XP_011511541.1:p.Pro552=
XM_006713789.3:c.2243_2244delinsCG	XP_006713852.1:p.Pro748=
XM_017007324.1:c.2243_2244delinsCG	XP_016862813.1:p.Pro748=
XM_017007325.1:c.2243_2244delinsCG	XP_016862814.1:p.Pro748=
NM_000388.4:c.2243_2244delinsCG MANE Select	NP_000379.3:p.Pro748=
NM_001178065.2:c.2273_2274delinsCG	NP_001171536.2:p.Pro758=