Canonical Allele Identifier: CA449827205
Gene: AGER HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32151516C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32183739C>A , CM000668.2:g.32183739C>A GRCh38
NC_000006.11:g.32151516C>A , CM000668.1:g.32151516C>A GRCh37
NC_000006.10:g.32259494C>A NCBI36
NG_029868.1:g.5584G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.171G>T MANE Select ENSP00000364217.4:p.Arg57=
ENST00000375055.6:c.171G>T ENSP00000364195.2:p.Arg57=
ENST00000375056.6:c.171G>T ENSP00000364196.2:p.Arg57=
ENST00000375065.6:c.-182+219G>T ENSP00000364206.6:n.-182+219G>T
ENST00000375067.7:c.160-31G>T ENSP00000364208.3:n.160-31G>T
ENST00000375069.7:c.171G>T ENSP00000364210.4:p.Arg57=
ENST00000375070.7:c.-133G>T ENSP00000364211.4:n.-133G>T
ENST00000375076.8:c.171G>T ENSP00000364217.4:p.Arg57=
ENST00000438221.6:c.171G>T ENSP00000387887.2:p.Arg57=
ENST00000450110.5:c.171G>T ENSP00000398466.1:p.Arg57=
ENST00000484849.5:n.378G>T
ENST00000538695.2:c.171G>T ENSP00000445389.1:p.Arg57=
ENST00000620802.4:c.171G>T ENSP00000484081.1:p.Arg57=
NM_001136.4:c.171G>T NP_001127.1:p.Arg57=
NM_001206929.1:c.171G>T NP_001193858.1:p.Arg57=
NM_001206932.1:c.160-31G>T NP_001193861.1:n.160-31G>T
NM_001206934.1:c.171G>T NP_001193863.1:p.Arg57=
NM_001206936.1:c.171G>T NP_001193865.1:p.Arg57=
NM_001206940.1:c.171G>T NP_001193869.1:p.Arg57=
NM_001206954.1:c.171G>T NP_001193883.1:p.Arg57=
NM_001206966.1:c.171G>T NP_001193895.1:p.Arg57=
NM_172197.2:c.160-31G>T NP_751947.1:n.160-31G>T
NR_038190.1:n.454G>T
XM_017010328.2:c.264G>T XP_016865817.1:p.Arg88=
XR_001743189.2:n.329G>T
XR_001743190.2:n.329G>T
NM_001136.5:c.171G>T MANE Select NP_001127.1:p.Arg57=
NM_001206932.2:c.160-31G>T NP_001193861.1:n.160-31G>T
NM_001206936.2:c.171G>T NP_001193865.1:p.Arg57=
NM_001206940.2:c.171G>T NP_001193869.1:p.Arg57=
NM_001206954.2:c.171G>T NP_001193883.1:p.Arg57=
NM_001206966.2:c.171G>T NP_001193895.1:p.Arg57=
NM_172197.3:c.160-31G>T NP_751947.1:n.160-31G>T
NR_038190.2:n.385G>T
NM_001206929.2:c.171G>T NP_001193858.1:p.Arg57=
NM_001206934.2:c.171G>T NP_001193863.1:p.Arg57=