Canonical Allele Identifier: CA363510989
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181621C>G , CM000668.2:g.32181621C>G GRCh38
NC_000006.11:g.32149398C>G , CM000668.1:g.32149398C>G GRCh37
NC_000006.10:g.32257376C>G NCBI36
NG_029868.1:g.7702G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.976G>C MANE Select ENSP00000364217.4:p.Glu326Gln
ENST00000375055.6:c.976G>C ENSP00000364195.2:p.Glu326Gln
ENST00000375065.6:c.163G>C ENSP00000364206.6:p.Glu55Gln
ENST00000375067.7:c.821G>C ENSP00000364208.3:p.Gly274Ala
ENST00000375069.7:c.1024G>C ENSP00000364210.4:p.Glu342Gln
ENST00000375070.7:c.662-144G>C ENSP00000364211.4:n.662-144G>C
ENST00000375076.8:c.976G>C ENSP00000364217.4:p.Glu326Gln
ENST00000438221.6:c.1024G>C ENSP00000387887.2:p.Glu342Gln
ENST00000469940.5:n.15G>C
ENST00000473619.5:n.518G>C
ENST00000484849.5:n.1183G>C
ENST00000488669.5:n.518G>C
ENST00000620802.4:c.283-188G>C ENSP00000484081.1:n.283-188G>C
NM_001136.4:c.976G>C NP_001127.1:p.Glu326Gln
NM_001206929.1:c.1024G>C NP_001193858.1:p.Glu342Gln
NM_001206932.1:c.934G>C NP_001193861.1:p.Glu312Gln
NM_001206934.1:c.1024G>C NP_001193863.1:p.Glu342Gln
NM_001206936.1:c.924G>C NP_001193865.1:p.Arg308Ser
NM_001206940.1:c.976G>C NP_001193869.1:p.Glu326Gln
NM_001206954.1:c.834G>C NP_001193883.1:p.Arg278Ser
NM_001206966.1:c.976G>C NP_001193895.1:p.Glu326Gln
NM_172197.2:c.821G>C NP_751947.1:p.Gly274Ala
NR_038190.1:n.1259G>C
XM_017010328.2:c.975G>C XP_016865817.1:p.Arg325Ser
XR_001743189.2:n.1040G>C
XR_001743190.2:n.992G>C
NM_001136.5:c.976G>C MANE Select NP_001127.1:p.Glu326Gln
NM_001206932.2:c.934G>C NP_001193861.1:p.Glu312Gln
NM_001206936.2:c.924G>C NP_001193865.1:p.Arg308Ser
NM_001206940.2:c.976G>C NP_001193869.1:p.Glu326Gln
NM_001206954.2:c.834G>C NP_001193883.1:p.Arg278Ser
NM_001206966.2:c.976G>C NP_001193895.1:p.Glu326Gln
NM_172197.3:c.821G>C NP_751947.1:p.Gly274Ala
NR_038190.2:n.1190G>C
NM_001206929.2:c.1024G>C NP_001193858.1:p.Glu342Gln
NM_001206934.2:c.1024G>C NP_001193863.1:p.Glu342Gln