Canonical Allele Identifier: CA363510002
Gene: AGER HGNC NCBI

Linked Data

dbSNP Id: rs2127432915

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181400G>C , CM000668.2:g.32181400G>C GRCh38
NC_000006.11:g.32149177G>C , CM000668.1:g.32149177G>C GRCh37
NC_000006.10:g.32257155G>C NCBI36
NG_029868.1:g.7923C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375076.9:c.1069C>G MANE Select ENSP00000364217.4:p.Leu357Val
ENST00000375055.6:c.*29+124C>G ENSP00000364195.2:n.*29+124C>G
ENST00000375065.6:c.256C>G ENSP00000364206.6:p.Leu86Val
ENST00000375067.7:c.914C>G ENSP00000364208.3:p.Ala305Gly
ENST00000375069.7:c.1117C>G ENSP00000364210.4:p.Leu373Val
ENST00000375070.7:c.739C>G ENSP00000364211.4:p.Leu247Val
ENST00000375076.8:c.1069C>G ENSP00000364217.4:p.Leu357Val
ENST00000438221.6:c.*29+124C>G ENSP00000387887.2:n.*29+124C>G
ENST00000469940.5:n.236C>G
ENST00000473619.5:n.611C>G
ENST00000484849.5:n.1276C>G
ENST00000488669.5:n.615+124C>G
ENST00000620802.4:c.316C>G ENSP00000484081.1:p.Leu106Val
NM_001136.4:c.1069C>G NP_001127.1:p.Leu357Val
NM_001206929.1:c.1117C>G NP_001193858.1:p.Leu373Val
NM_001206932.1:c.1027C>G NP_001193861.1:p.Leu343Val
NM_001206934.1:c.*29+124C>G NP_001193863.1:n.*29+124C>G
NM_001206936.1:c.1021+124C>G NP_001193865.1:n.1021+124C>G
NM_001206940.1:c.*29+124C>G NP_001193869.1:n.*29+124C>G
NM_001206954.1:c.931+124C>G NP_001193883.1:n.931+124C>G
NM_001206966.1:c.*29+124C>G NP_001193895.1:n.*29+124C>G
NM_172197.2:c.914C>G NP_751947.1:p.Ala305Gly
NR_038190.1:n.1352C>G
XM_017010328.2:c.1072+124C>G XP_016865817.1:n.1072+124C>G
XR_001743189.2:n.1133C>G
XR_001743190.2:n.1085C>G
NM_001136.5:c.1069C>G MANE Select NP_001127.1:p.Leu357Val
NM_001206932.2:c.1027C>G NP_001193861.1:p.Leu343Val
NM_001206936.2:c.1021+124C>G NP_001193865.1:n.1021+124C>G
NM_001206940.2:c.*29+124C>G NP_001193869.1:n.*29+124C>G
NM_001206954.2:c.931+124C>G NP_001193883.1:n.931+124C>G
NM_001206966.2:c.*29+124C>G NP_001193895.1:n.*29+124C>G
NM_172197.3:c.914C>G NP_751947.1:p.Ala305Gly
NR_038190.2:n.1283C>G
NM_001206929.2:c.1117C>G NP_001193858.1:p.Leu373Val
NM_001206934.2:c.*29+124C>G NP_001193863.1:n.*29+124C>G