Canonical Allele Identifier: CA2650971193

Gene: AGT

Linked Data

• gnomAD v4: 1-230705941-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705941_230705942insCC , CM000663.2:g.230705941_230705942insCC	GRCh38
NC_000001.10:g.230841687_230841688insCC , CM000663.1:g.230841687_230841688insCC	GRCh37
NC_000001.9:g.228908310_228908311insCC	NCBI36
NG_008836.1:g.13649_13650insGG
NG_008836.2:g.13649_13650insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1088_1089insGG MANE Select	ENSP00000355627.5:p.Ser364AspfsTer8
ENST00000679684.1:c.1088_1089insGG	ENSP00000505981.1:p.Ser364AspfsTer8
ENST00000679738.1:c.1088_1089insGG	ENSP00000505063.1:p.Ser364AspfsTer8
ENST00000679802.1:c.*547_*548insGG	ENSP00000505184.1:n.*547_*548insGG
ENST00000679854.1:n.5393_5394insGG
ENST00000679957.1:c.1088_1089insGG	ENSP00000506646.1:p.Ser364AspfsTer8
ENST00000680041.1:c.1088_1089insGG	ENSP00000504866.1:p.Ser364AspfsTer8
ENST00000680783.1:c.829+4053_829+4054insGG	ENSP00000506329.1:n.829+4053_829+4054insG...
ENST00000681269.1:c.1088_1089insGG	ENSP00000505985.1:p.Ser364AspfsTer8
ENST00000681347.1:n.1599_1600insGG
ENST00000681514.1:c.1088_1089insGG	ENSP00000505963.1:p.Ser364AspfsTer8
ENST00000681772.1:c.1088_1089insGG	ENSP00000505829.1:p.Ser364AspfsTer?
ENST00000366667.4:c.1115_1116insGG	ENSP00000355627.4:p.Ser373AspfsTer8
NM_000029.3:c.1115_1116insGG	NP_000020.1:p.Ser373AspfsTer8
NM_000029.4:c.1115_1116insGG	NP_000020.1:p.Ser373AspfsTer8
NM_001382817.3:c.1088_1089insGG	NP_001369746.2:p.Ser364AspfsTer8
NM_001384479.1:c.1088_1089insGG MANE Select	NP_001371408.1:p.Ser364AspfsTer8