Canonical Allele Identifier: CA363510639
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181581T>A , CM000668.2:g.32181581T>A GRCh38
NC_000006.11:g.32149358T>A , CM000668.1:g.32149358T>A GRCh37
NC_000006.10:g.32257336T>A NCBI36
NG_029868.1:g.7742A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.991+25A>T MANE Select ENSP00000364217.4:n.991+25A>T
ENST00000375055.6:c.1016A>T ENSP00000364195.2:p.Glu339Val
ENST00000375065.6:c.178+25A>T ENSP00000364206.6:n.178+25A>T
ENST00000375067.7:c.836+25A>T ENSP00000364208.3:n.836+25A>T
ENST00000375069.7:c.1039+25A>T ENSP00000364210.4:n.1039+25A>T
ENST00000375070.7:c.662-104A>T ENSP00000364211.4:n.662-104A>T
ENST00000375076.8:c.991+25A>T ENSP00000364217.4:n.991+25A>T
ENST00000438221.6:c.1064A>T ENSP00000387887.2:p.Glu355Val
ENST00000469940.5:n.55A>T
ENST00000473619.5:n.533+25A>T
ENST00000484849.5:n.1198+25A>T
ENST00000488669.5:n.558A>T
ENST00000620802.4:c.283-148A>T ENSP00000484081.1:n.283-148A>T
NM_001136.4:c.991+25A>T NP_001127.1:n.991+25A>T
NM_001206929.1:c.1039+25A>T NP_001193858.1:n.1039+25A>T
NM_001206932.1:c.949+25A>T NP_001193861.1:n.949+25A>T
NM_001206934.1:c.1064A>T NP_001193863.1:p.Glu355Val
NM_001206936.1:c.964A>T NP_001193865.1:p.Lys322Ter
NM_001206940.1:c.1016A>T NP_001193869.1:p.Glu339Val
NM_001206954.1:c.874A>T NP_001193883.1:p.Lys292Ter
NM_001206966.1:c.1016A>T NP_001193895.1:p.Glu339Val
NM_172197.2:c.836+25A>T NP_751947.1:n.836+25A>T
NR_038190.1:n.1274+25A>T
XM_017010328.2:c.1015A>T XP_016865817.1:p.Lys339Ter
XR_001743189.2:n.1055+25A>T
XR_001743190.2:n.1007+25A>T
NM_001136.5:c.991+25A>T MANE Select NP_001127.1:n.991+25A>T
NM_001206932.2:c.949+25A>T NP_001193861.1:n.949+25A>T
NM_001206936.2:c.964A>T NP_001193865.1:p.Lys322Ter
NM_001206940.2:c.1016A>T NP_001193869.1:p.Glu339Val
NM_001206954.2:c.874A>T NP_001193883.1:p.Lys292Ter
NM_001206966.2:c.1016A>T NP_001193895.1:p.Glu339Val
NM_172197.3:c.836+25A>T NP_751947.1:n.836+25A>T
NR_038190.2:n.1205+25A>T
NM_001206929.2:c.1039+25A>T NP_001193858.1:n.1039+25A>T
NM_001206934.2:c.1064A>T NP_001193863.1:p.Glu355Val