Canonical Allele Identifier: CA2586972876

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284645dup , CM000665.2:g.122284645dup	GRCh38
NC_000003.11:g.122003492dup , CM000665.1:g.122003492dup	GRCh37
NC_000003.10:g.123486182dup	NCBI36
NG_009058.1:g.105963dup
NG_009058.2:g.105978dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2460dup	ENSP00000418685.2:p.Arg821AlafsTer?
ENST00000498619.4:c.2721dup	ENSP00000420194.1:p.Arg908AlafsTer?
ENST00000638421.1:c.2691dup	ENSP00000492190.1:p.Arg898AlafsTer?
ENST00000639785.2:c.2691dup MANE Select	ENSP00000491584.2:p.Arg898AlafsTer?
ENST00000490131.5:c.2691dup	ENSP00000418685.1:p.Arg898AlafsTer?
ENST00000498619.2:c.2721dup	ENSP00000420194.1:p.Arg908AlafsTer?
NM_000388.3:c.2691dup	NP_000379.2:p.Arg898AlafsTer?
NM_001178065.1:c.2721dup	NP_001171536.1:p.Arg908AlafsTer?
XM_005247836.2:c.2691dup	XP_005247893.1:p.Arg898AlafsTer?
XM_005247837.2:c.2208dup	XP_005247894.1:p.Arg737AlafsTer?
XM_006713789.2:c.2691dup	XP_006713852.1:p.Arg898AlafsTer?
XM_011513237.1:c.2691dup	XP_011511539.1:p.Arg898AlafsTer?
XM_011513238.1:c.2691dup	XP_011511540.1:p.Arg898AlafsTer?
XM_011513239.1:c.2103dup	XP_011511541.1:p.Arg702AlafsTer?
XM_006713789.3:c.2691dup	XP_006713852.1:p.Arg898AlafsTer?
XM_017007324.1:c.2691dup	XP_016862813.1:p.Arg898AlafsTer?
XM_017007325.1:c.2691dup	XP_016862814.1:p.Arg898AlafsTer?
NM_000388.4:c.2691dup MANE Select	NP_000379.3:p.Arg898AlafsTer?
NM_001178065.2:c.2721dup	NP_001171536.2:p.Arg908AlafsTer?