Canonical Allele Identifier: CA363509967
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181394C>G , CM000668.2:g.32181394C>G GRCh38
NC_000006.11:g.32149171C>G , CM000668.1:g.32149171C>G GRCh37
NC_000006.10:g.32257149C>G NCBI36
NG_029868.1:g.7929G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375076.9:c.1075G>C MANE Select ENSP00000364217.4:p.Gly359Arg
ENST00000375055.6:c.*29+130G>C ENSP00000364195.2:n.*29+130G>C
ENST00000375065.6:c.262G>C ENSP00000364206.6:p.Gly88Arg
ENST00000375067.7:c.920G>C ENSP00000364208.3:p.Trp307Ser
ENST00000375069.7:c.1123G>C ENSP00000364210.4:p.Gly375Arg
ENST00000375070.7:c.745G>C ENSP00000364211.4:p.Gly249Arg
ENST00000375076.8:c.1075G>C ENSP00000364217.4:p.Gly359Arg
ENST00000438221.6:c.*29+130G>C ENSP00000387887.2:n.*29+130G>C
ENST00000469940.5:n.242G>C
ENST00000473619.5:n.617G>C
ENST00000484849.5:n.1282G>C
ENST00000488669.5:n.615+130G>C
ENST00000620802.4:c.322G>C ENSP00000484081.1:p.Gly108Arg
NM_001136.4:c.1075G>C NP_001127.1:p.Gly359Arg
NM_001206929.1:c.1123G>C NP_001193858.1:p.Gly375Arg
NM_001206932.1:c.1033G>C NP_001193861.1:p.Gly345Arg
NM_001206934.1:c.*29+130G>C NP_001193863.1:n.*29+130G>C
NM_001206936.1:c.1021+130G>C NP_001193865.1:n.1021+130G>C
NM_001206940.1:c.*29+130G>C NP_001193869.1:n.*29+130G>C
NM_001206954.1:c.931+130G>C NP_001193883.1:n.931+130G>C
NM_001206966.1:c.*29+130G>C NP_001193895.1:n.*29+130G>C
NM_172197.2:c.920G>C NP_751947.1:p.Trp307Ser
NR_038190.1:n.1358G>C
XM_017010328.2:c.1072+130G>C XP_016865817.1:n.1072+130G>C
XR_001743189.2:n.1139G>C
XR_001743190.2:n.1091G>C
NM_001136.5:c.1075G>C MANE Select NP_001127.1:p.Gly359Arg
NM_001206932.2:c.1033G>C NP_001193861.1:p.Gly345Arg
NM_001206936.2:c.1021+130G>C NP_001193865.1:n.1021+130G>C
NM_001206940.2:c.*29+130G>C NP_001193869.1:n.*29+130G>C
NM_001206954.2:c.931+130G>C NP_001193883.1:n.931+130G>C
NM_001206966.2:c.*29+130G>C NP_001193895.1:n.*29+130G>C
NM_172197.3:c.920G>C NP_751947.1:p.Trp307Ser
NR_038190.2:n.1289G>C
NM_001206929.2:c.1123G>C NP_001193858.1:p.Gly375Arg
NM_001206934.2:c.*29+130G>C NP_001193863.1:n.*29+130G>C