Canonical Allele Identifier: CA898108821

Gene: CASR

Linked Data

• dbSNP Id: rs1480980328
• MyVariant Identifiers: chr3:g.122000578_122000584del (hg19) ; chr3:g.122281731_122281737del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122281734_122281740del , CM000665.2:g.122281734_122281740del	GRCh38
NC_000003.11:g.122000581_122000587del , CM000665.1:g.122000581_122000587del	GRCh37
NC_000003.10:g.123483271_123483277del	NCBI36
NG_009058.1:g.103052_103058del
NG_009058.2:g.103067_103073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1378-379_1378-373del	ENSP00000418685.2:n.1378-379_1378-373del
ENST00000498619.4:c.1609-349_1609-343del	ENSP00000420194.1:n.1609-349_1609-343del
ENST00000638421.1:c.1609-379_1609-373del	ENSP00000492190.1:n.1609-379_1609-373del
ENST00000639785.2:c.1609-379_1609-373del MANE Select	ENSP00000491584.2:n.1609-379_1609-373del
ENST00000490131.5:c.1609-379_1609-373del	ENSP00000418685.1:n.1609-379_1609-373del
ENST00000498619.2:c.1609-349_1609-343del	ENSP00000420194.1:n.1609-349_1609-343del
NM_000388.3:c.1609-379_1609-373del	NP_000379.2:n.1609-379_1609-373del
NM_001178065.1:c.1609-349_1609-343del	NP_001171536.1:n.1609-349_1609-343del
XM_005247836.2:c.1609-379_1609-373del	XP_005247893.1:n.1609-379_1609-373del
XM_005247837.2:c.1126-379_1126-373del	XP_005247894.1:n.1126-379_1126-373del
XM_006713789.2:c.1609-379_1609-373del	XP_006713852.1:n.1609-379_1609-373del
XM_011513237.1:c.1609-379_1609-373del	XP_011511539.1:n.1609-379_1609-373del
XM_011513238.1:c.1609-379_1609-373del	XP_011511540.1:n.1609-379_1609-373del
XM_011513239.1:c.1021-379_1021-373del	XP_011511541.1:n.1021-379_1021-373del
XM_006713789.3:c.1609-379_1609-373del	XP_006713852.1:n.1609-379_1609-373del
XM_017007324.1:c.1609-379_1609-373del	XP_016862813.1:n.1609-379_1609-373del
XM_017007325.1:c.1609-379_1609-373del	XP_016862814.1:n.1609-379_1609-373del
NM_000388.4:c.1609-379_1609-373del MANE Select	NP_000379.3:n.1609-379_1609-373del
NM_001178065.2:c.1609-349_1609-343del	NP_001171536.2:n.1609-349_1609-343del