Canonical Allele Identifier: CA1619453144
Gene: AGER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32183744C= , CM000668.2:g.32183744C= GRCh38
NC_000006.11:g.32151521C= , CM000668.1:g.32151521C= GRCh37
NC_000006.10:g.32259499C= NCBI36
NG_029868.1:g.5579G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.166G= MANE Select ENSP00000364217.4:p.Gly56=
ENST00000375055.6:c.166G= ENSP00000364195.2:p.Gly56=
ENST00000375056.6:c.166G= ENSP00000364196.2:p.Gly56=
ENST00000375065.6:c.-182+214G= ENSP00000364206.6:n.-182+214G=
ENST00000375067.7:c.160-36G= ENSP00000364208.3:n.160-36G=
ENST00000375069.7:c.166G= ENSP00000364210.4:p.Gly56=
ENST00000375070.7:c.-138G= ENSP00000364211.4:n.-138G=
ENST00000375076.8:c.166G= ENSP00000364217.4:p.Gly56=
ENST00000438221.6:c.166G= ENSP00000387887.2:p.Gly56=
ENST00000450110.5:c.166G= ENSP00000398466.1:p.Gly56=
ENST00000484849.5:n.373G=
ENST00000538695.2:c.166G= ENSP00000445389.1:p.Gly56=
ENST00000620802.4:c.166G= ENSP00000484081.1:p.Gly56=
NM_001136.4:c.166G= NP_001127.1:p.Gly56=
NM_001206929.1:c.166G= NP_001193858.1:p.Gly56=
NM_001206932.1:c.160-36G= NP_001193861.1:n.160-36G=
NM_001206934.1:c.166G= NP_001193863.1:p.Gly56=
NM_001206936.1:c.166G= NP_001193865.1:p.Gly56=
NM_001206940.1:c.166G= NP_001193869.1:p.Gly56=
NM_001206954.1:c.166G= NP_001193883.1:p.Gly56=
NM_001206966.1:c.166G= NP_001193895.1:p.Gly56=
NM_172197.2:c.160-36G= NP_751947.1:n.160-36G=
NR_038190.1:n.449G=
XM_017010328.2:c.259G= XP_016865817.1:p.Gly87=
XR_001743189.2:n.324G=
XR_001743190.2:n.324G=
NM_001136.5:c.166G= MANE Select NP_001127.1:p.Gly56=
NM_001206932.2:c.160-36G= NP_001193861.1:n.160-36G=
NM_001206936.2:c.166G= NP_001193865.1:p.Gly56=
NM_001206940.2:c.166G= NP_001193869.1:p.Gly56=
NM_001206954.2:c.166G= NP_001193883.1:p.Gly56=
NM_001206966.2:c.166G= NP_001193895.1:p.Gly56=
NM_172197.3:c.160-36G= NP_751947.1:n.160-36G=
NR_038190.2:n.380G=
NM_001206929.2:c.166G= NP_001193858.1:p.Gly56=
NM_001206934.2:c.166G= NP_001193863.1:p.Gly56=