Canonical Allele Identifier: CA1619451397

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181544_32181545delinsTC , CM000668.2:g.32181544_32181545delinsTC	GRCh38
NC_000006.11:g.32149321_32149322delinsTC , CM000668.1:g.32149321_32149322delinsTC	GRCh37
NC_000006.10:g.32257299_32257300delinsTC	NCBI36
NG_029868.1:g.7778_7779delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.991+61_991+62delinsGA MANE Select	ENSP00000364217.4:n.991+61_991+62delinsGA
ENST00000375055.6:c.*8_*9delinsGA	ENSP00000364195.2:n.*8_*9delinsGA
ENST00000375065.6:c.178+61_178+62delinsGA	ENSP00000364206.6:n.178+61_178+62delinsGA
ENST00000375067.7:c.836+61_836+62delinsGA	ENSP00000364208.3:n.836+61_836+62delinsGA
ENST00000375069.7:c.1039+61_1039+62delinsGA	ENSP00000364210.4:n.1039+61_1039+62delinsGA
ENST00000375070.7:c.662-68_662-67delinsGA	ENSP00000364211.4:n.662-68_662-67delinsGA
ENST00000375076.8:c.991+61_991+62delinsGA	ENSP00000364217.4:n.991+61_991+62delinsGA
ENST00000438221.6:c.*8_*9delinsGA	ENSP00000387887.2:n.*8_*9delinsGA
ENST00000469940.5:n.91_92delinsGA
ENST00000473619.5:n.533+61_533+62delinsGA
ENST00000484849.5:n.1198+61_1198+62delinsGA
ENST00000488669.5:n.594_595delinsGA
ENST00000620802.4:c.283-112_283-111delinsGA	ENSP00000484081.1:n.283-112_283-111delinsGA
NM_001136.4:c.991+61_991+62delinsGA	NP_001127.1:n.991+61_991+62delinsGA
NM_001206929.1:c.1039+61_1039+62delinsGA	NP_001193858.1:n.1039+61_1039+62delinsGA
NM_001206932.1:c.949+61_949+62delinsGA	NP_001193861.1:n.949+61_949+62delinsGA
NM_001206934.1:c.*8_*9delinsGA	NP_001193863.1:n.*8_*9delinsGA
NM_001206936.1:c.1000_1001delinsGA	NP_001193865.1:p.Asp334=
NM_001206940.1:c.*8_*9delinsGA	NP_001193869.1:n.*8_*9delinsGA
NM_001206954.1:c.910_911delinsGA	NP_001193883.1:p.Asp304=
NM_001206966.1:c.*8_*9delinsGA	NP_001193895.1:n.*8_*9delinsGA
NM_172197.2:c.836+61_836+62delinsGA	NP_751947.1:n.836+61_836+62delinsGA
NR_038190.1:n.1274+61_1274+62delinsGA
XM_017010328.2:c.1051_1052delinsGA	XP_016865817.1:p.Asp351=
XR_001743189.2:n.1055+61_1055+62delinsGA
XR_001743190.2:n.1007+61_1007+62delinsGA
NM_001136.5:c.991+61_991+62delinsGA MANE Select	NP_001127.1:n.991+61_991+62delinsGA
NM_001206932.2:c.949+61_949+62delinsGA	NP_001193861.1:n.949+61_949+62delinsGA
NM_001206936.2:c.1000_1001delinsGA	NP_001193865.1:p.Asp334=
NM_001206940.2:c.*8_*9delinsGA	NP_001193869.1:n.*8_*9delinsGA
NM_001206954.2:c.910_911delinsGA	NP_001193883.1:p.Asp304=
NM_001206966.2:c.*8_*9delinsGA	NP_001193895.1:n.*8_*9delinsGA
NM_172197.3:c.836+61_836+62delinsGA	NP_751947.1:n.836+61_836+62delinsGA
NR_038190.2:n.1205+61_1205+62delinsGA
NM_001206929.2:c.1039+61_1039+62delinsGA	NP_001193858.1:n.1039+61_1039+62delinsGA
NM_001206934.2:c.*8_*9delinsGA	NP_001193863.1:n.*8_*9delinsGA