Canonical Allele Identifier: CA363510843
Gene: AGER HGNC NCBI

Linked Data

dbSNP Id: rs764928579
gnomAD v4: 6-32181605-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181605C>T , CM000668.2:g.32181605C>T GRCh38
NC_000006.11:g.32149382C>T , CM000668.1:g.32149382C>T GRCh37
NC_000006.10:g.32257360C>T NCBI36
NG_029868.1:g.7718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.991+1G>A MANE Select ENSP00000364217.4:n.991+1G>A
ENST00000375055.6:c.992G>A ENSP00000364195.2:p.Gly331Asp
ENST00000375065.6:c.178+1G>A ENSP00000364206.6:n.178+1G>A
ENST00000375067.7:c.836+1G>A ENSP00000364208.3:n.836+1G>A
ENST00000375069.7:c.1039+1G>A ENSP00000364210.4:n.1039+1G>A
ENST00000375070.7:c.662-128G>A ENSP00000364211.4:n.662-128G>A
ENST00000375076.8:c.991+1G>A ENSP00000364217.4:n.991+1G>A
ENST00000438221.6:c.1040G>A ENSP00000387887.2:p.Gly347Asp
ENST00000469940.5:n.31G>A
ENST00000473619.5:n.533+1G>A
ENST00000484849.5:n.1198+1G>A
ENST00000488669.5:n.534G>A
ENST00000620802.4:c.283-172G>A ENSP00000484081.1:n.283-172G>A
NM_001136.4:c.991+1G>A NP_001127.1:n.991+1G>A
NM_001206929.1:c.1039+1G>A NP_001193858.1:n.1039+1G>A
NM_001206932.1:c.949+1G>A NP_001193861.1:n.949+1G>A
NM_001206934.1:c.1040G>A NP_001193863.1:p.Gly347Asp
NM_001206936.1:c.940G>A NP_001193865.1:p.Val314Met
NM_001206940.1:c.992G>A NP_001193869.1:p.Gly331Asp
NM_001206954.1:c.850G>A NP_001193883.1:p.Val284Met
NM_001206966.1:c.992G>A NP_001193895.1:p.Gly331Asp
NM_172197.2:c.836+1G>A NP_751947.1:n.836+1G>A
NR_038190.1:n.1274+1G>A
XM_017010328.2:c.991G>A XP_016865817.1:p.Val331Met
XR_001743189.2:n.1055+1G>A
XR_001743190.2:n.1007+1G>A
NM_001136.5:c.991+1G>A MANE Select NP_001127.1:n.991+1G>A
NM_001206932.2:c.949+1G>A NP_001193861.1:n.949+1G>A
NM_001206936.2:c.940G>A NP_001193865.1:p.Val314Met
NM_001206940.2:c.992G>A NP_001193869.1:p.Gly331Asp
NM_001206954.2:c.850G>A NP_001193883.1:p.Val284Met
NM_001206966.2:c.992G>A NP_001193895.1:p.Gly331Asp
NM_172197.3:c.836+1G>A NP_751947.1:n.836+1G>A
NR_038190.2:n.1205+1G>A
NM_001206929.2:c.1039+1G>A NP_001193858.1:n.1039+1G>A
NM_001206934.2:c.1040G>A NP_001193863.1:p.Gly347Asp