Canonical Allele Identifier: CA2770520136

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181632_32181672del , CM000668.2:g.32181632_32181672del	GRCh38
NC_000006.11:g.32149409_32149449del , CM000668.1:g.32149409_32149449del	GRCh37
NC_000006.10:g.32257387_32257427del	NCBI36
NG_029868.1:g.7651_7691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.965-40_965del
ENST00000375055.6:c.965-40_965del
ENST00000375065.6:c.152-40_152del
ENST00000375067.7:c.810-40_810del
ENST00000375069.7:c.1013-40_1013del
ENST00000375070.7:c.662-195_662-155del	ENSP00000364211.4:n.662-195_662-155del
ENST00000375076.8:c.965-40_965del
ENST00000438221.6:c.1013-40_1013del
ENST00000473619.5:n.507-40_507del
ENST00000484849.5:n.1172-40_1172del
ENST00000488669.5:n.507-40_507del
ENST00000620802.4:c.283-239_283-199del	ENSP00000484081.1:n.283-239_283-199del
NM_001136.4:c.965-40_965del
NM_001206929.1:c.1013-40_1013del
NM_001206932.1:c.923-40_923del
NM_001206934.1:c.1013-40_1013del
NM_001206936.1:c.913-40_913del
NM_001206940.1:c.965-40_965del
NM_001206954.1:c.823-40_823del
NM_001206966.1:c.965-40_965del
NM_172197.2:c.810-40_810del
NR_038190.1:n.1248-40_1248del
XM_017010328.2:c.964-40_964del
XR_001743189.2:n.1029-40_1029del
XR_001743190.2:n.981-40_981del
NM_001136.5:c.965-40_965del
NM_001206932.2:c.923-40_923del
NM_001206936.2:c.913-40_913del
NM_001206940.2:c.965-40_965del
NM_001206954.2:c.823-40_823del
NM_001206966.2:c.965-40_965del
NM_172197.3:c.810-40_810del
NR_038190.2:n.1179-40_1179del
NM_001206929.2:c.1013-40_1013del
NM_001206934.2:c.1013-40_1013del