Canonical Allele Identifier: CA2650971169

Gene: AGT

Linked Data

• gnomAD v4: 1-230705861-TCCCCACCCCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705867_230705877del , CM000663.2:g.230705867_230705877del	GRCh38
NC_000001.10:g.230841613_230841623del , CM000663.1:g.230841613_230841623del	GRCh37
NC_000001.9:g.228908236_228908246del	NCBI36
NG_008836.1:g.13719_13729del
NG_008836.2:g.13719_13729del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+61_1097+71del MANE Select	ENSP00000355627.5:n.1097+61_1097+71del
ENST00000679684.1:c.1097+61_1097+71del	ENSP00000505981.1:n.1097+61_1097+71del
ENST00000679738.1:c.1097+61_1097+71del	ENSP00000505063.1:n.1097+61_1097+71del
ENST00000679802.1:c.*556+61_*556+71del	ENSP00000505184.1:n.*556+61_*556+71del
ENST00000679854.1:n.5402+61_5402+71del
ENST00000679957.1:c.1097+61_1097+71del	ENSP00000506646.1:n.1097+61_1097+71del
ENST00000680041.1:c.1097+61_1097+71del	ENSP00000504866.1:n.1097+61_1097+71del
ENST00000680783.1:c.829+4123_829+4133del	ENSP00000506329.1:n.829+4123_829+4133del
ENST00000681269.1:c.1097+61_1097+71del	ENSP00000505985.1:n.1097+61_1097+71del
ENST00000681347.1:n.1669_1679del
ENST00000681514.1:c.1097+61_1097+71del	ENSP00000505963.1:n.1097+61_1097+71del
ENST00000681772.1:c.*57_*67del	ENSP00000505829.1:n.*57_*67del
ENST00000366667.4:c.1124+61_1124+71del	ENSP00000355627.4:n.1124+61_1124+71del
NM_000029.3:c.1124+61_1124+71del	NP_000020.1:n.1124+61_1124+71del
NM_000029.4:c.1124+61_1124+71del	NP_000020.1:n.1124+61_1124+71del
NM_001382817.3:c.1097+61_1097+71del	NP_001369746.2:n.1097+61_1097+71del
NM_001384479.1:c.1097+61_1097+71del MANE Select	NP_001371408.1:n.1097+61_1097+71del