Canonical Allele Identifier: CA1619451389
Gene: AGER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181522A= , CM000668.2:g.32181522A= GRCh38
NC_000006.11:g.32149299A= , CM000668.1:g.32149299A= GRCh37
NC_000006.10:g.32257277A= NCBI36
NG_029868.1:g.7801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.992-45T= MANE Select ENSP00000364217.4:n.992-45T=
ENST00000375055.6:c.*29+2T= ENSP00000364195.2:n.*29+2T=
ENST00000375065.6:c.179-45T= ENSP00000364206.6:n.179-45T=
ENST00000375067.7:c.837-45T= ENSP00000364208.3:n.837-45T=
ENST00000375069.7:c.1040-45T= ENSP00000364210.4:n.1040-45T=
ENST00000375070.7:c.662-45T= ENSP00000364211.4:n.662-45T=
ENST00000375076.8:c.992-45T= ENSP00000364217.4:n.992-45T=
ENST00000438221.6:c.*29+2T= ENSP00000387887.2:n.*29+2T=
ENST00000469940.5:n.114T=
ENST00000473619.5:n.534-45T=
ENST00000484849.5:n.1199-45T=
ENST00000488669.5:n.615+2T=
ENST00000620802.4:c.283-89T= ENSP00000484081.1:n.283-89T=
NM_001136.4:c.992-45T= NP_001127.1:n.992-45T=
NM_001206929.1:c.1040-45T= NP_001193858.1:n.1040-45T=
NM_001206932.1:c.950-45T= NP_001193861.1:n.950-45T=
NM_001206934.1:c.*29+2T= NP_001193863.1:n.*29+2T=
NM_001206936.1:c.1021+2T= NP_001193865.1:n.1021+2T=
NM_001206940.1:c.*29+2T= NP_001193869.1:n.*29+2T=
NM_001206954.1:c.931+2T= NP_001193883.1:n.931+2T=
NM_001206966.1:c.*29+2T= NP_001193895.1:n.*29+2T=
NM_172197.2:c.837-45T= NP_751947.1:n.837-45T=
NR_038190.1:n.1275-45T=
XM_017010328.2:c.1072+2T= XP_016865817.1:n.1072+2T=
XR_001743189.2:n.1056-45T=
XR_001743190.2:n.1008-45T=
NM_001136.5:c.992-45T= MANE Select NP_001127.1:n.992-45T=
NM_001206932.2:c.950-45T= NP_001193861.1:n.950-45T=
NM_001206936.2:c.1021+2T= NP_001193865.1:n.1021+2T=
NM_001206940.2:c.*29+2T= NP_001193869.1:n.*29+2T=
NM_001206954.2:c.931+2T= NP_001193883.1:n.931+2T=
NM_001206966.2:c.*29+2T= NP_001193895.1:n.*29+2T=
NM_172197.3:c.837-45T= NP_751947.1:n.837-45T=
NR_038190.2:n.1206-45T=
NM_001206929.2:c.1040-45T= NP_001193858.1:n.1040-45T=
NM_001206934.2:c.*29+2T= NP_001193863.1:n.*29+2T=