Canonical Allele Identifier: CA2578576784
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181660_32181663del , CM000668.2:g.32181660_32181663del GRCh38
NC_000006.11:g.32149437_32149440del , CM000668.1:g.32149437_32149440del GRCh37
NC_000006.10:g.32257415_32257418del NCBI36
NG_029868.1:g.7662_7665del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.965-29_965-26del MANE Select ENSP00000364217.4:n.965-29_965-26del
ENST00000375055.6:c.965-29_965-26del ENSP00000364195.2:n.965-29_965-26del
ENST00000375065.6:c.152-29_152-26del ENSP00000364206.6:n.152-29_152-26del
ENST00000375067.7:c.810-29_810-26del ENSP00000364208.3:n.810-29_810-26del
ENST00000375069.7:c.1013-29_1013-26del ENSP00000364210.4:n.1013-29_1013-26del
ENST00000375070.7:c.662-184_662-181del ENSP00000364211.4:n.662-184_662-181del
ENST00000375076.8:c.965-29_965-26del ENSP00000364217.4:n.965-29_965-26del
ENST00000438221.6:c.1013-29_1013-26del ENSP00000387887.2:n.1013-29_1013-26del
ENST00000473619.5:n.507-29_507-26del
ENST00000484849.5:n.1172-29_1172-26del
ENST00000488669.5:n.507-29_507-26del
ENST00000620802.4:c.283-228_283-225del ENSP00000484081.1:n.283-228_283-225del
NM_001136.4:c.965-29_965-26del NP_001127.1:n.965-29_965-26del
NM_001206929.1:c.1013-29_1013-26del NP_001193858.1:n.1013-29_1013-26del
NM_001206932.1:c.923-29_923-26del NP_001193861.1:n.923-29_923-26del
NM_001206934.1:c.1013-29_1013-26del NP_001193863.1:n.1013-29_1013-26del
NM_001206936.1:c.913-29_913-26del NP_001193865.1:n.913-29_913-26del
NM_001206940.1:c.965-29_965-26del NP_001193869.1:n.965-29_965-26del
NM_001206954.1:c.823-29_823-26del NP_001193883.1:n.823-29_823-26del
NM_001206966.1:c.965-29_965-26del NP_001193895.1:n.965-29_965-26del
NM_172197.2:c.810-29_810-26del NP_751947.1:n.810-29_810-26del
NR_038190.1:n.1248-29_1248-26del
XM_017010328.2:c.964-29_964-26del XP_016865817.1:n.964-29_964-26del
XR_001743189.2:n.1029-29_1029-26del
XR_001743190.2:n.981-29_981-26del
NM_001136.5:c.965-29_965-26del MANE Select NP_001127.1:n.965-29_965-26del
NM_001206932.2:c.923-29_923-26del NP_001193861.1:n.923-29_923-26del
NM_001206936.2:c.913-29_913-26del NP_001193865.1:n.913-29_913-26del
NM_001206940.2:c.965-29_965-26del NP_001193869.1:n.965-29_965-26del
NM_001206954.2:c.823-29_823-26del NP_001193883.1:n.823-29_823-26del
NM_001206966.2:c.965-29_965-26del NP_001193895.1:n.965-29_965-26del
NM_172197.3:c.810-29_810-26del NP_751947.1:n.810-29_810-26del
NR_038190.2:n.1179-29_1179-26del
NM_001206929.2:c.1013-29_1013-26del NP_001193858.1:n.1013-29_1013-26del
NM_001206934.2:c.1013-29_1013-26del NP_001193863.1:n.1013-29_1013-26del