Canonical Allele Identifier: CA2667224461

Gene: CASR

Linked Data

• gnomAD v4: 3-122257688-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122257688_122257689insAC , CM000665.2:g.122257688_122257689insAC	GRCh38
NC_000003.11:g.121976535_121976536insAC , CM000665.1:g.121976535_121976536insAC	GRCh37
NC_000003.10:g.123459225_123459226insAC	NCBI36
NG_009058.1:g.79006_79007insAC
NG_009058.2:g.79021_79022insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.492+301_492+302insAC	ENSP00000418685.2:n.492+301_492+302insAC
ENST00000498619.4:c.492+301_492+302insAC	ENSP00000420194.1:n.492+301_492+302insAC
ENST00000638421.1:c.492+301_492+302insAC	ENSP00000492190.1:n.492+301_492+302insAC
ENST00000639785.2:c.492+301_492+302insAC MANE Select	ENSP00000491584.2:n.492+301_492+302insAC
ENST00000490131.5:c.492+301_492+302insAC	ENSP00000418685.1:n.492+301_492+302insAC
ENST00000498619.2:c.492+301_492+302insAC	ENSP00000420194.1:n.492+301_492+302insAC
NM_000388.3:c.492+301_492+302insAC	NP_000379.2:n.492+301_492+302insAC
NM_001178065.1:c.492+301_492+302insAC	NP_001171536.1:n.492+301_492+302insAC
XM_005247836.2:c.492+301_492+302insAC	XP_005247893.1:n.492+301_492+302insAC
XM_005247837.2:c.9+3314_9+3315insAC	XP_005247894.1:n.9+3314_9+3315insAC
XM_006713789.2:c.492+301_492+302insAC	XP_006713852.1:n.492+301_492+302insAC
XM_011513237.1:c.492+301_492+302insAC	XP_011511539.1:n.492+301_492+302insAC
XM_011513238.1:c.492+301_492+302insAC	XP_011511540.1:n.492+301_492+302insAC
XM_006713789.3:c.492+301_492+302insAC	XP_006713852.1:n.492+301_492+302insAC
XM_017007324.1:c.492+301_492+302insAC	XP_016862813.1:n.492+301_492+302insAC
XM_017007325.1:c.492+301_492+302insAC	XP_016862814.1:n.492+301_492+302insAC
NM_000388.4:c.492+301_492+302insAC MANE Select	NP_000379.3:n.492+301_492+302insAC
NM_001178065.2:c.492+301_492+302insAC	NP_001171536.2:n.492+301_492+302insAC