Canonical Allele Identifier: CA363509761
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181355C>A , CM000668.2:g.32181355C>A GRCh38
NC_000006.11:g.32149132C>A , CM000668.1:g.32149132C>A GRCh37
NC_000006.10:g.32257110C>A NCBI36
NG_029868.1:g.7968G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.1114G>T MANE Select ENSP00000364217.4:p.Glu372Ter
ENST00000375055.6:c.*30-116G>T ENSP00000364195.2:n.*30-116G>T
ENST00000375065.6:c.301G>T ENSP00000364206.6:p.Glu101Ter
ENST00000375067.7:c.959G>T ENSP00000364208.3:p.Gly320Val
ENST00000375069.7:c.1162G>T ENSP00000364210.4:p.Glu388Ter
ENST00000375070.7:c.784G>T ENSP00000364211.4:p.Glu262Ter
ENST00000375076.8:c.1114G>T ENSP00000364217.4:p.Glu372Ter
ENST00000438221.6:c.*30-116G>T ENSP00000387887.2:n.*30-116G>T
ENST00000469940.5:n.281G>T
ENST00000473619.5:n.656G>T
ENST00000484849.5:n.1321G>T
ENST00000488669.5:n.616-116G>T
ENST00000620802.4:c.361G>T ENSP00000484081.1:p.Glu121Ter
NM_001136.4:c.1114G>T NP_001127.1:p.Glu372Ter
NM_001206929.1:c.1162G>T NP_001193858.1:p.Glu388Ter
NM_001206932.1:c.1072G>T NP_001193861.1:p.Glu358Ter
NM_001206934.1:c.*30-116G>T NP_001193863.1:n.*30-116G>T
NM_001206936.1:c.1022-116G>T NP_001193865.1:n.1022-116G>T
NM_001206940.1:c.*30-116G>T NP_001193869.1:n.*30-116G>T
NM_001206954.1:c.932-116G>T NP_001193883.1:n.932-116G>T
NM_001206966.1:c.*29+169G>T NP_001193895.1:n.*29+169G>T
NM_172197.2:c.959G>T NP_751947.1:p.Gly320Val
NR_038190.1:n.1397G>T
XM_017010328.2:c.1073-116G>T XP_016865817.1:n.1073-116G>T
XR_001743189.2:n.1178G>T
XR_001743190.2:n.1130G>T
NM_001136.5:c.1114G>T MANE Select NP_001127.1:p.Glu372Ter
NM_001206932.2:c.1072G>T NP_001193861.1:p.Glu358Ter
NM_001206936.2:c.1022-116G>T NP_001193865.1:n.1022-116G>T
NM_001206940.2:c.*30-116G>T NP_001193869.1:n.*30-116G>T
NM_001206954.2:c.932-116G>T NP_001193883.1:n.932-116G>T
NM_001206966.2:c.*29+169G>T NP_001193895.1:n.*29+169G>T
NM_172197.3:c.959G>T NP_751947.1:p.Gly320Val
NR_038190.2:n.1328G>T
NM_001206929.2:c.1162G>T NP_001193858.1:p.Glu388Ter
NM_001206934.2:c.*30-116G>T NP_001193863.1:n.*30-116G>T