Canonical Allele Identifier: CA363509728
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181349A>T , CM000668.2:g.32181349A>T GRCh38
NC_000006.11:g.32149126A>T , CM000668.1:g.32149126A>T GRCh37
NC_000006.10:g.32257104A>T NCBI36
NG_029868.1:g.7974T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.1118+2T>A MANE Select ENSP00000364217.4:n.1118+2T>A
ENST00000375055.6:c.*30-110T>A ENSP00000364195.2:n.*30-110T>A
ENST00000375065.6:c.305+2T>A ENSP00000364206.6:n.305+2T>A
ENST00000375067.7:c.963+2T>A ENSP00000364208.3:n.963+2T>A
ENST00000375069.7:c.1166+2T>A ENSP00000364210.4:n.1166+2T>A
ENST00000375070.7:c.788+2T>A ENSP00000364211.4:n.788+2T>A
ENST00000375076.8:c.1118+2T>A ENSP00000364217.4:n.1118+2T>A
ENST00000438221.6:c.*30-110T>A ENSP00000387887.2:n.*30-110T>A
ENST00000469940.5:n.285+2T>A
ENST00000473619.5:n.660+2T>A
ENST00000484849.5:n.1325+2T>A
ENST00000488669.5:n.616-110T>A
ENST00000620802.4:c.365+2T>A ENSP00000484081.1:n.365+2T>A
NM_001136.4:c.1118+2T>A NP_001127.1:n.1118+2T>A
NM_001206929.1:c.1166+2T>A NP_001193858.1:n.1166+2T>A
NM_001206932.1:c.1076+2T>A NP_001193861.1:n.1076+2T>A
NM_001206934.1:c.*30-110T>A NP_001193863.1:n.*30-110T>A
NM_001206936.1:c.1022-110T>A NP_001193865.1:n.1022-110T>A
NM_001206940.1:c.*30-110T>A NP_001193869.1:n.*30-110T>A
NM_001206954.1:c.932-110T>A NP_001193883.1:n.932-110T>A
NM_001206966.1:c.*29+175T>A NP_001193895.1:n.*29+175T>A
NM_172197.2:c.963+2T>A NP_751947.1:n.963+2T>A
NR_038190.1:n.1401+2T>A
XM_017010328.2:c.1073-110T>A XP_016865817.1:n.1073-110T>A
XR_001743189.2:n.1182+2T>A
XR_001743190.2:n.1134+2T>A
NM_001136.5:c.1118+2T>A MANE Select NP_001127.1:n.1118+2T>A
NM_001206932.2:c.1076+2T>A NP_001193861.1:n.1076+2T>A
NM_001206936.2:c.1022-110T>A NP_001193865.1:n.1022-110T>A
NM_001206940.2:c.*30-110T>A NP_001193869.1:n.*30-110T>A
NM_001206954.2:c.932-110T>A NP_001193883.1:n.932-110T>A
NM_001206966.2:c.*29+175T>A NP_001193895.1:n.*29+175T>A
NM_172197.3:c.963+2T>A NP_751947.1:n.963+2T>A
NR_038190.2:n.1332+2T>A
NM_001206929.2:c.1166+2T>A NP_001193858.1:n.1166+2T>A
NM_001206934.2:c.*30-110T>A NP_001193863.1:n.*30-110T>A