Canonical Allele Identifier: CA1087507363
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181739_32181740insTTTT , CM000668.2:g.32181739_32181740insTTTT GRCh38
NC_000006.11:g.32149516_32149517insTTTT , CM000668.1:g.32149516_32149517insTTTT GRCh37
NC_000006.10:g.32257494_32257495insTTTT NCBI36
NG_029868.1:g.7584_7585insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.965-107_965-106insAAAA MANE Select ENSP00000364217.4:n.965-107_965-106insAAAA
ENST00000375055.6:c.965-107_965-106insAAAA ENSP00000364195.2:n.965-107_965-106insAAAA
ENST00000375065.6:c.152-107_152-106insAAAA ENSP00000364206.6:n.152-107_152-106insAAAA
ENST00000375067.7:c.810-107_810-106insAAAA ENSP00000364208.3:n.810-107_810-106insAAAA
ENST00000375069.7:c.1013-107_1013-106insAAAA ENSP00000364210.4:n.1013-107_1013-106insAAAA
ENST00000375070.7:c.662-262_662-261insAAAA ENSP00000364211.4:n.662-262_662-261insAAAA
ENST00000375076.8:c.965-107_965-106insAAAA ENSP00000364217.4:n.965-107_965-106insAAAA
ENST00000438221.6:c.1013-107_1013-106insAAAA ENSP00000387887.2:n.1013-107_1013-106insAAAA
ENST00000473619.5:n.507-107_507-106insAAAA
ENST00000484849.5:n.1172-107_1172-106insAAAA
ENST00000488669.5:n.507-107_507-106insAAAA
ENST00000620802.4:c.283-306_283-305insAAAA ENSP00000484081.1:n.283-306_283-305insAAAA
NM_001136.4:c.965-107_965-106insAAAA NP_001127.1:n.965-107_965-106insAAAA
NM_001206929.1:c.1013-107_1013-106insAAAA NP_001193858.1:n.1013-107_1013-106insAAAA
NM_001206932.1:c.923-107_923-106insAAAA NP_001193861.1:n.923-107_923-106insAAAA
NM_001206934.1:c.1013-107_1013-106insAAAA NP_001193863.1:n.1013-107_1013-106insAAAA
NM_001206936.1:c.913-107_913-106insAAAA NP_001193865.1:n.913-107_913-106insAAAA
NM_001206940.1:c.965-107_965-106insAAAA NP_001193869.1:n.965-107_965-106insAAAA
NM_001206954.1:c.823-107_823-106insAAAA NP_001193883.1:n.823-107_823-106insAAAA
NM_001206966.1:c.965-107_965-106insAAAA NP_001193895.1:n.965-107_965-106insAAAA
NM_172197.2:c.810-107_810-106insAAAA NP_751947.1:n.810-107_810-106insAAAA
NR_038190.1:n.1248-107_1248-106insAAAA
XM_017010328.2:c.964-107_964-106insAAAA XP_016865817.1:n.964-107_964-106insAAAA
XR_001743189.2:n.1029-107_1029-106insAAAA
XR_001743190.2:n.981-107_981-106insAAAA
NM_001136.5:c.965-107_965-106insAAAA MANE Select NP_001127.1:n.965-107_965-106insAAAA
NM_001206932.2:c.923-107_923-106insAAAA NP_001193861.1:n.923-107_923-106insAAAA
NM_001206936.2:c.913-107_913-106insAAAA NP_001193865.1:n.913-107_913-106insAAAA
NM_001206940.2:c.965-107_965-106insAAAA NP_001193869.1:n.965-107_965-106insAAAA
NM_001206954.2:c.823-107_823-106insAAAA NP_001193883.1:n.823-107_823-106insAAAA
NM_001206966.2:c.965-107_965-106insAAAA NP_001193895.1:n.965-107_965-106insAAAA
NM_172197.3:c.810-107_810-106insAAAA NP_751947.1:n.810-107_810-106insAAAA
NR_038190.2:n.1179-107_1179-106insAAAA
NM_001206929.2:c.1013-107_1013-106insAAAA NP_001193858.1:n.1013-107_1013-106insAAAA
NM_001206934.2:c.1013-107_1013-106insAAAA NP_001193863.1:n.1013-107_1013-106insAAAA