Canonical Allele Identifier: CA363510019
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181403G>T , CM000668.2:g.32181403G>T GRCh38
NC_000006.11:g.32149180G>T , CM000668.1:g.32149180G>T GRCh37
NC_000006.10:g.32257158G>T NCBI36
NG_029868.1:g.7920C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375076.9:c.1066C>A MANE Select ENSP00000364217.4:p.Leu356Met
ENST00000375055.6:c.*29+121C>A ENSP00000364195.2:n.*29+121C>A
ENST00000375065.6:c.253C>A ENSP00000364206.6:p.Leu85Met
ENST00000375067.7:c.911C>A ENSP00000364208.3:p.Pro304His
ENST00000375069.7:c.1114C>A ENSP00000364210.4:p.Leu372Met
ENST00000375070.7:c.736C>A ENSP00000364211.4:p.Leu246Met
ENST00000375076.8:c.1066C>A ENSP00000364217.4:p.Leu356Met
ENST00000438221.6:c.*29+121C>A ENSP00000387887.2:n.*29+121C>A
ENST00000469940.5:n.233C>A
ENST00000473619.5:n.608C>A
ENST00000484849.5:n.1273C>A
ENST00000488669.5:n.615+121C>A
ENST00000620802.4:c.313C>A ENSP00000484081.1:p.Leu105Met
NM_001136.4:c.1066C>A NP_001127.1:p.Leu356Met
NM_001206929.1:c.1114C>A NP_001193858.1:p.Leu372Met
NM_001206932.1:c.1024C>A NP_001193861.1:p.Leu342Met
NM_001206934.1:c.*29+121C>A NP_001193863.1:n.*29+121C>A
NM_001206936.1:c.1021+121C>A NP_001193865.1:n.1021+121C>A
NM_001206940.1:c.*29+121C>A NP_001193869.1:n.*29+121C>A
NM_001206954.1:c.931+121C>A NP_001193883.1:n.931+121C>A
NM_001206966.1:c.*29+121C>A NP_001193895.1:n.*29+121C>A
NM_172197.2:c.911C>A NP_751947.1:p.Pro304His
NR_038190.1:n.1349C>A
XM_017010328.2:c.1072+121C>A XP_016865817.1:n.1072+121C>A
XR_001743189.2:n.1130C>A
XR_001743190.2:n.1082C>A
NM_001136.5:c.1066C>A MANE Select NP_001127.1:p.Leu356Met
NM_001206932.2:c.1024C>A NP_001193861.1:p.Leu342Met
NM_001206936.2:c.1021+121C>A NP_001193865.1:n.1021+121C>A
NM_001206940.2:c.*29+121C>A NP_001193869.1:n.*29+121C>A
NM_001206954.2:c.931+121C>A NP_001193883.1:n.931+121C>A
NM_001206966.2:c.*29+121C>A NP_001193895.1:n.*29+121C>A
NM_172197.3:c.911C>A NP_751947.1:p.Pro304His
NR_038190.2:n.1280C>A
NM_001206929.2:c.1114C>A NP_001193858.1:p.Leu372Met
NM_001206934.2:c.*29+121C>A NP_001193863.1:n.*29+121C>A