Canonical Allele Identifier: CA2667225249

Gene: CASR

Linked Data

• gnomAD v4: 3-122262448-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122262448_122262449insG , CM000665.2:g.122262448_122262449insG	GRCh38
NC_000003.11:g.121981295_121981296insG , CM000665.1:g.121981295_121981296insG	GRCh37
NC_000003.10:g.123463985_123463986insG	NCBI36
NG_009058.1:g.83766_83767insG
NG_009058.2:g.83781_83782insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1377+36_1377+37insG	ENSP00000418685.2:n.1377+36_1377+37insG
ENST00000498619.4:c.1377+36_1377+37insG	ENSP00000420194.1:n.1377+36_1377+37insG
ENST00000638421.1:c.1377+36_1377+37insG	ENSP00000492190.1:n.1377+36_1377+37insG
ENST00000639785.2:c.1377+36_1377+37insG MANE Select	ENSP00000491584.2:n.1377+36_1377+37insG
ENST00000490131.5:c.1377+36_1377+37insG	ENSP00000418685.1:n.1377+36_1377+37insG
ENST00000498619.2:c.1377+36_1377+37insG	ENSP00000420194.1:n.1377+36_1377+37insG
NM_000388.3:c.1377+36_1377+37insG	NP_000379.2:n.1377+36_1377+37insG
NM_001178065.1:c.1377+36_1377+37insG	NP_001171536.1:n.1377+36_1377+37insG
XM_005247836.2:c.1377+36_1377+37insG	XP_005247893.1:n.1377+36_1377+37insG
XM_005247837.2:c.894+36_894+37insG	XP_005247894.1:n.894+36_894+37insG
XM_006713789.2:c.1377+36_1377+37insG	XP_006713852.1:n.1377+36_1377+37insG
XM_011513237.1:c.1377+36_1377+37insG	XP_011511539.1:n.1377+36_1377+37insG
XM_011513238.1:c.1377+36_1377+37insG	XP_011511540.1:n.1377+36_1377+37insG
XM_011513239.1:c.789+36_789+37insG	XP_011511541.1:n.789+36_789+37insG
XM_006713789.3:c.1377+36_1377+37insG	XP_006713852.1:n.1377+36_1377+37insG
XM_017007324.1:c.1377+36_1377+37insG	XP_016862813.1:n.1377+36_1377+37insG
XM_017007325.1:c.1377+36_1377+37insG	XP_016862814.1:n.1377+36_1377+37insG
NM_000388.4:c.1377+36_1377+37insG MANE Select	NP_000379.3:n.1377+36_1377+37insG
NM_001178065.2:c.1377+36_1377+37insG	NP_001171536.2:n.1377+36_1377+37insG