Canonical Allele Identifier: CA136916115
Gene: AGER HGNC NCBI

Linked Data

dbSNP Id: rs900321363
gnomAD v3: 6-32183616-C-T
gnomAD v4: 6-32183616-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32183616C>T , CM000668.2:g.32183616C>T GRCh38
NC_000006.11:g.32151393C>T , CM000668.1:g.32151393C>T GRCh37
NC_000006.10:g.32259371C>T NCBI36
NG_029868.1:g.5707G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.294G>A MANE Select ENSP00000364217.4:p.Arg98=
ENST00000375055.6:c.294G>A ENSP00000364195.2:p.Arg98=
ENST00000375056.6:c.294G>A ENSP00000364196.2:p.Arg98=
ENST00000375065.6:c.-182+342G>A ENSP00000364206.6:n.-182+342G>A
ENST00000375067.7:c.252G>A ENSP00000364208.3:p.Arg84=
ENST00000375069.7:c.294G>A ENSP00000364210.4:p.Arg98=
ENST00000375070.7:c.-10G>A ENSP00000364211.4:n.-10G>A
ENST00000375076.8:c.294G>A ENSP00000364217.4:p.Arg98=
ENST00000438221.6:c.294G>A ENSP00000387887.2:p.Arg98=
ENST00000450110.5:c.294G>A ENSP00000398466.1:p.Arg98=
ENST00000484849.5:n.501G>A
ENST00000538695.2:c.294G>A ENSP00000445389.1:p.Arg98=
ENST00000620802.4:c.282+12G>A ENSP00000484081.1:n.282+12G>A
NM_001136.4:c.294G>A NP_001127.1:p.Arg98=
NM_001206929.1:c.294G>A NP_001193858.1:p.Arg98=
NM_001206932.1:c.252G>A NP_001193861.1:p.Arg84=
NM_001206934.1:c.294G>A NP_001193863.1:p.Arg98=
NM_001206936.1:c.294G>A NP_001193865.1:p.Arg98=
NM_001206940.1:c.294G>A NP_001193869.1:p.Arg98=
NM_001206954.1:c.294G>A NP_001193883.1:p.Arg98=
NM_001206966.1:c.294G>A NP_001193895.1:p.Arg98=
NM_172197.2:c.252G>A NP_751947.1:p.Arg84=
NR_038190.1:n.577G>A
XM_017010328.2:c.387G>A XP_016865817.1:p.Arg129=
XR_001743189.2:n.452G>A
XR_001743190.2:n.452G>A
NM_001136.5:c.294G>A MANE Select NP_001127.1:p.Arg98=
NM_001206932.2:c.252G>A NP_001193861.1:p.Arg84=
NM_001206936.2:c.294G>A NP_001193865.1:p.Arg98=
NM_001206940.2:c.294G>A NP_001193869.1:p.Arg98=
NM_001206954.2:c.294G>A NP_001193883.1:p.Arg98=
NM_001206966.2:c.294G>A NP_001193895.1:p.Arg98=
NM_172197.3:c.252G>A NP_751947.1:p.Arg84=
NR_038190.2:n.508G>A
NM_001206929.2:c.294G>A NP_001193858.1:p.Arg98=
NM_001206934.2:c.294G>A NP_001193863.1:p.Arg98=