Canonical Allele Identifier: CA1226667772

Gene: AGT

Linked Data

• dbSNP Id: rs1663371759

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705940_230705941insCAGGGAGGC , CM000663.2:g.230705940_230705941insCAGGGAGGC	GRCh38
NC_000001.10:g.230841686_230841687insCAGGGAGGC , CM000663.1:g.230841686_230841687insCAGGGAGGC	GRCh37
NC_000001.9:g.228908309_228908310insCAGGGAGGC	NCBI36
NG_008836.1:g.13650_13651insGCCTCCCTG
NG_008836.2:g.13650_13651insGCCTCCCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1089_1090insGCCTCCCTG MANE Select	ENSP00000355627.5:p.Leu363_Ser364insAlaSe...
ENST00000679684.1:c.1089_1090insGCCTCCCTG	ENSP00000505981.1:p.Leu363_Ser364insAlaSe...
ENST00000679738.1:c.1089_1090insGCCTCCCTG	ENSP00000505063.1:p.Leu363_Ser364insAlaSe...
ENST00000679802.1:c.*548_*549insGCCTCCCTG	ENSP00000505184.1:n.*548_*549insGCCTCCCTG...
ENST00000679854.1:n.5394_5395insGCCTCCCTG
ENST00000679957.1:c.1089_1090insGCCTCCCTG	ENSP00000506646.1:p.Leu363_Ser364insAlaSe...
ENST00000680041.1:c.1089_1090insGCCTCCCTG	ENSP00000504866.1:p.Leu363_Ser364insAlaSe...
ENST00000680783.1:c.829+4054_829+4055insGCCTCCCTG	ENSP00000506329.1:n.829+4054_829+4055insG...
ENST00000681269.1:c.1089_1090insGCCTCCCTG	ENSP00000505985.1:p.Leu363_Ser364insAlaSe...
ENST00000681347.1:n.1600_1601insGCCTCCCTG
ENST00000681514.1:c.1089_1090insGCCTCCCTG	ENSP00000505963.1:p.Leu363_Ser364insAlaSe...
ENST00000681772.1:c.1089_1090insGCCTCCCTG	ENSP00000505829.1:p.Leu363_Ser364insAlaSe...
ENST00000366667.4:c.1116_1117insGCCTCCCTG	ENSP00000355627.4:p.Leu372_Ser373insAlaSe...
NM_000029.3:c.1116_1117insGCCTCCCTG	NP_000020.1:p.Leu372_Ser373insAlaSerLeu
NM_000029.4:c.1116_1117insGCCTCCCTG	NP_000020.1:p.Leu372_Ser373insAlaSerLeu
NM_001382817.3:c.1089_1090insGCCTCCCTG	NP_001369746.2:p.Leu363_Ser364insAlaSerLe...
NM_001384479.1:c.1089_1090insGCCTCCCTG MANE Select	NP_001371408.1:p.Leu363_Ser364insAlaSerLe...