Canonical Allele Identifier: CA354161544

Gene: CASR

Linked Data

• gnomAD v4: 3-122285090-G-T
• MyVariant Identifiers: chr3:g.122003937G>T (hg19) ; chr3:g.122285090G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122285090G>T , CM000665.2:g.122285090G>T	GRCh38
NC_000003.11:g.122003937G>T , CM000665.1:g.122003937G>T	GRCh37
NC_000003.10:g.123486627G>T	NCBI36
NG_009058.1:g.106408G>T
NG_009058.2:g.106423G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.2905G>T	ENSP00000418685.2:p.Asp969Tyr
ENST00000498619.4:c.3166G>T	ENSP00000420194.1:p.Asp1056Tyr
ENST00000638421.1:c.3136G>T	ENSP00000492190.1:p.Asp1046Tyr
ENST00000639785.2:c.3136G>T MANE Select	ENSP00000491584.2:p.Asp1046Tyr
ENST00000490131.5:c.3136G>T	ENSP00000418685.1:p.Asp1046Tyr
ENST00000498619.2:c.3166G>T	ENSP00000420194.1:p.Asp1056Tyr
NM_000388.3:c.3136G>T	NP_000379.2:p.Asp1046Tyr
NM_001178065.1:c.3166G>T	NP_001171536.1:p.Asp1056Tyr
XM_005247836.2:c.3136G>T	XP_005247893.1:p.Asp1046Tyr
XM_005247837.2:c.2653G>T	XP_005247894.1:p.Asp885Tyr
XM_006713789.2:c.3136G>T	XP_006713852.1:p.Asp1046Tyr
XM_011513237.1:c.3136G>T	XP_011511539.1:p.Asp1046Tyr
XM_011513238.1:c.3136G>T	XP_011511540.1:p.Asp1046Tyr
XM_011513239.1:c.2548G>T	XP_011511541.1:p.Asp850Tyr
XM_006713789.3:c.3136G>T	XP_006713852.1:p.Asp1046Tyr
XM_017007324.1:c.3136G>T	XP_016862813.1:p.Asp1046Tyr
XM_017007325.1:c.3136G>T	XP_016862814.1:p.Asp1046Tyr
NM_000388.4:c.3136G>T MANE Select	NP_000379.3:p.Asp1046Tyr
NM_001178065.2:c.3166G>T	NP_001171536.2:p.Asp1056Tyr