Canonical Allele Identifier: CA363510585
Gene: AGER HGNC NCBI

Linked Data

gnomAD v4: 6-32181574-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181574T>G , CM000668.2:g.32181574T>G GRCh38
NC_000006.11:g.32149351T>G , CM000668.1:g.32149351T>G GRCh37
NC_000006.10:g.32257329T>G NCBI36
NG_029868.1:g.7749A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.991+32A>C MANE Select ENSP00000364217.4:n.991+32A>C
ENST00000375055.6:c.1023A>C ENSP00000364195.2:p.Glu341Asp
ENST00000375065.6:c.178+32A>C ENSP00000364206.6:n.178+32A>C
ENST00000375067.7:c.836+32A>C ENSP00000364208.3:n.836+32A>C
ENST00000375069.7:c.1039+32A>C ENSP00000364210.4:n.1039+32A>C
ENST00000375070.7:c.662-97A>C ENSP00000364211.4:n.662-97A>C
ENST00000375076.8:c.991+32A>C ENSP00000364217.4:n.991+32A>C
ENST00000438221.6:c.1071A>C ENSP00000387887.2:p.Glu357Asp
ENST00000469940.5:n.62A>C
ENST00000473619.5:n.533+32A>C
ENST00000484849.5:n.1198+32A>C
ENST00000488669.5:n.565A>C
ENST00000620802.4:c.283-141A>C ENSP00000484081.1:n.283-141A>C
NM_001136.4:c.991+32A>C NP_001127.1:n.991+32A>C
NM_001206929.1:c.1039+32A>C NP_001193858.1:n.1039+32A>C
NM_001206932.1:c.949+32A>C NP_001193861.1:n.949+32A>C
NM_001206934.1:c.1071A>C NP_001193863.1:p.Glu357Asp
NM_001206936.1:c.971A>C NP_001193865.1:p.Lys324Thr
NM_001206940.1:c.1023A>C NP_001193869.1:p.Glu341Asp
NM_001206954.1:c.881A>C NP_001193883.1:p.Lys294Thr
NM_001206966.1:c.1023A>C NP_001193895.1:p.Glu341Asp
NM_172197.2:c.836+32A>C NP_751947.1:n.836+32A>C
NR_038190.1:n.1274+32A>C
XM_017010328.2:c.1022A>C XP_016865817.1:p.Lys341Thr
XR_001743189.2:n.1055+32A>C
XR_001743190.2:n.1007+32A>C
NM_001136.5:c.991+32A>C MANE Select NP_001127.1:n.991+32A>C
NM_001206932.2:c.949+32A>C NP_001193861.1:n.949+32A>C
NM_001206936.2:c.971A>C NP_001193865.1:p.Lys324Thr
NM_001206940.2:c.1023A>C NP_001193869.1:p.Glu341Asp
NM_001206954.2:c.881A>C NP_001193883.1:p.Lys294Thr
NM_001206966.2:c.1023A>C NP_001193895.1:p.Glu341Asp
NM_172197.3:c.836+32A>C NP_751947.1:n.836+32A>C
NR_038190.2:n.1205+32A>C
NM_001206929.2:c.1039+32A>C NP_001193858.1:n.1039+32A>C
NM_001206934.2:c.1071A>C NP_001193863.1:p.Glu357Asp