Canonical Allele Identifier: CA2519577113

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704285_230704398del , CM000663.2:g.230704285_230704398del	GRCh38
NC_000001.10:g.230840031_230840144del , CM000663.1:g.230840031_230840144del	GRCh37
NC_000001.9:g.228906654_228906767del	NCBI36
NG_008836.1:g.15193_15306del
NG_008836.2:g.15193_15306del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1098-61_1150del
ENST00000679684.1:c.1098-61_1150del
ENST00000679738.1:c.1098-61_1150del
ENST00000679802.1:c.*557-61_*609del
ENST00000679854.1:n.5403-61_5455del
ENST00000679957.1:c.1098-61_1150del
ENST00000680041.1:c.1098-61_1150del
ENST00000680783.1:c.829+5597_829+5710del	ENSP00000506329.1:n.829+5597_829+5710del
ENST00000681269.1:c.1098-61_1150del
ENST00000681347.1:n.3143_3256del
ENST00000681514.1:c.1098-61_1150del
ENST00000681772.1:c.*592-61_*644del
ENST00000366667.4:c.1125-61_1177del
NM_000029.3:c.1125-61_1177del
NM_000029.4:c.1125-61_1177del
NM_001382817.3:c.1098-61_1150del
NM_001384479.1:c.1098-61_1150del